Form 26 For Drug Manufacturing License: Fill & Download for Free

How to get a manufacturing licence for hand made soaps?As per the Drugs and Cosmetics Act and Rule, the Central Government and the State Government makes rule regarding issuance of licence to a person for manufacturing cosmetics. Basically it is the State Drug Authorities of respective States, who are authorized to issue manufacturing licenses.Firstly, a person applying for a manufacturing licence for hand made soap needs to fill the application form 31 along with it; the person is required to pay an amount of Rs 3,500 and Rs 2,500 as a government and inspection fee of 2500 respectively.Secondly, the cosmetics for which the licence is being acquired should be specified into classes of cosmetics, as has been mentioned under Schedule M-II, where the cosmetics have been classified into 10 categories.A person applying for the license of manufacturing hand made soap or any other cosmetics should have passed intermediate exam with Chemistry as one of its subject or any examination which is recognised by the Licensing authority.Apart from it to get a license it is required to hold a diploma in Pharmacy which should be certified and approved either under the Pharmacy Council of India under the Pharmacy Act, 1948 or under the Pharmacy Act, 1948At the time of applying for the licence it is required to mention other information like the lists of equipment, manufacturing facility details with minimum area required for manufacturing, Technical Competent personnel details, etc.Apart from those details the licencing authority also considers before approving the licence that whether the cosmetic is misbranded or is a spurious cosmetic.For renewal also the manufacturer is required to categorise the cosmetics as per Schedule M-II, apart from it Rs. 1000 has to be paid as a charge for every inspection for renewalIt is mandatory for the Licensing Authority to direct an inspection of the area where manufacturing will take place, before approving or rejecting the application of license. After the inspection a report is send to the Licensing Authority on the basis of which they either approve the licence application or reject it.Place of ManufacturingWhile determining the place for manufacturing the hand made soaps it has to be seen that the manufacturing house should work in a manner it benefits the public at the same time it should not affect the environment adversely. Also there has been rule laid down relating to the factory premises which have been mentioned in the Schedule M-II of the Drugs and Cosmetics Act and Rule. The manufacturer has to comply with those requirements and conditions.Location and surroundings– The production house or factory should not be established near residential areas. Also it should have measures to avoid risk of contamination from the external environment including open sewage, drain, and public lavatory.Building and premises– ventilation openings and similar lines shall be designed Apart from it the factory should have proper sanitation facilities, hygiene should be maintain in the manufacturing building, for that it has to be ensured that the workers are provided and are using hand gloves and masks. They shall also conform to the conditions laid down in the factories Act, 1948. They should design, construct and maintain to prevent the entry of insects, pests, birds and rodents.Waste disposal– Proper arrangement should be made for disposal of solid waste as well as liquid waste. All bio-medical waste shall be destroyed as per the provisions of the Bio-Medical Waste Rule, 1996. Apart from it provision should be made for proper and safe storage of waste material waiting for disposal.Health, clothing and sanitation of workers- prior to employment all personnel shall undergo medical examination including eye examination. It should be ensured that any of the working staff is not suffering from any communicable diseases. Also all the employ should be required to report about their illness or abnormal health condition to their immediate supervisor.Drugs Controller General is appointed by the Central Government as a head of the Central Drug Standard Control Organization who is authorised to regulate the cosmetics and drugs in India.Action which can be taken when the manufacturing of hand made soap is against the provisions of Drugs and Cosmetics Acts and RulesThe act provides provisions for penalising the manufacturer who does not comply with the Act, which has been dealt under Sec.26 to Sec.29 of the Act, by manufacturing cosmetics which are prohibited by the Act, or is not disclosing the name of manufacturer, place of manufacturing, any other records or documents prescribed by the legitimate authority. The person may either be imprisoned or may be fined or both. The fine may exceed upto Rs. 5000. Also a person is penalised if uses any report of a test or analysis which the Central Drugs Laboratory or Government Analyst has given.Import and export of the hand made soapsFor a manufacturer to import hand made soap has to fill form 10. As per the new amendment 2010, it is required to have prior registration before importation of any cosmetic to India, which includes hand made soap. The Central Government has the power to prohibit the import of cosmetics in public interest only. If the Central Government is satisfied that the use would harm the public then it can prohibit the import of the cosmetics.The Central Drug Standard Control Organization also controls the import of cosmetics and drugs at the same time regulate the approval of new drugs. The basic requirement for the import and export of the hand soap are Manufacturing license, good Manufacturing Practice (GMP), Free sale Certificates, labelling of a cosmetic is required for bot importing and exporting of a cosmetic. Labelling should be done as per the methods prescribed under Rule 148 of the Drug and Cosmetic Act, the product should not contain prohibited items as prescribed by the Act and the hand soap should either comply with the Bureau of Indian Standards or of the International Cosmetics Standards.ConclusionIncrease in manufacturing house for hand made soaps on one hand fulfils the demand of the public and on the other hand it also generates employment opportunities. The Act not only deals with the licencing process but also deals with import and export of the hand soap; it also looks into the working of the manufacturing department. The Act gives power to the Central and State Government to check the working these manufacturing companies after they get licence. Hence, the Central government establishes different committees under this Act like Drug Technical Advisory Board who advises the Central Government as well as the State Government on matters arising out of the Administration of the Act. A Central Drugs Laboratory is also established by the Central Government in order to determine the working of the manufacturing company that they comply with the Act or not.

LOAN LICENCING is a pure business arrangement and all normal business regulations will apply.You will have to enter into a loan/ licence manufacturing agreement with the facility/ factory owner________________LOAN LICENCING in Pharmaceutical Manufacturing is the term used for getting manufactured own product at other’s premises at LOAN LICENCE contract.LOAN LICENCING is just like hiring/ renting others manufacturing premises for manufacturing owns products.LOAN LICENCING require two parties: One is marketing company and second one is manufacturing company.In LOAN LICENCING marketing company can use its company name at place of manufactured by address but address will of manufacturer’s company premises.It is similar to third party manufacturing but has few differences.In LOAN LICENCING you can use marketed by address and manufactured by name of your company.LOAN LICENCE: Under Drugs and Cosmetics Rules, A Loan license is defined as “For the purpose of this rule a LOAN LICENCE means a license which a licensing authority may issue to an applicant who does not have his own arrangements for manufacture but who intends to avail himself of the manufacturing facilities owned by a licensee in FORM 25 or in FORM 28 as the case may be.”____________________________LABELLING REQUIREMENTS ARE AS FOR PROBIOTICSSchedule – X (See regulation 10) List of Strains as Probiotics (Live Micro- organisms) 1 Lactobacillus acidophilus 2 Lactobacillus planatrum 3 Lactobacillus reuteri 4 Lactobacillus rhamnosus 5 Lactobacillus salivarius 6 Lactobacillus casei 7 Lactobasillus brevis 8 Lactobacillus infantis 9 Lactobacillus johnsonii 10 Lactobacillus bulgaricans 11 Lactobacillus asporogenes 12 Lactobacillus fermentis 13 Lactobacillus caucasicus 14 Lactobacillus helvetucs 15 Lactobacillus lactis 16 Lactobacillus amylovorus 17 Lactobacillus gallanarum 18 Lactobacillus debrueckii 19 Bifidobacterium bifidum 20 Bifidobacterium lactis 21 Bifidobacterium breve 22 Bifidobacterium longum 23 Bifidbacterium animalis 24 Bifidbacterium infontis 25 Streptococcus thermophilus 26 Streptococcus bouraldi 27 Saccharomyces species (as in codex) PS: These organisms may be used either singly or in combination but must be declared on the label with full information and has to be non-GMO.Schedule – XI (See regulation 11) List of Prebiotic Compounds 1 Polydextrose 2 Soybean Oligosaccharides 3 Isomalto-oligosaccharides 4 Fructo-oligosaccharides 5 Gluco-oligosaccharides 6 Xylo-oligosaccharides 7 Inulin 8 Isomaltulose 9 Gentio-ologsaccharides 10 Lactulose 11 Lactoferrin 12 Sugar alcohols such as lactitol, sorbitol, maltitol, etc.____________________________For revised FEES/ FORMS update kindly refer to Website of Drug Controller etc.loan licence1[70A. Form of loan licence to manufacture for sale 2[or for distribution] of drugs other than those 3[specified in Schedules C, C (1) and X].—A loan licence to manufacture for sale 2[or for distribution] of drugs other than those specified in 2[Schedules C, C(1) and X] shall be issued in Form 25A.]73A. A certificate of renewal of loan licence—The certificate of renewal of a loan licence in Form 25A shall be issued in Form 26A.]73AA. Duration of loan licence—An original loan licence in Form 25A or renewed loan licence in Form 26A, unless sooner suspended or cancelled, shall be 1[valid for a period of five years on and from the date on which] it is granted or renewed:2[Provided that if the application for the renewal of a licence is made before its expiry or if the application is made within six months of its expiry, after payment of the additional fees, the licence shall continue to be in force until orders are passed on the application and the licence shall be deemed to have expired if the application for its renewal is not made within six months of its expiry.]1[75A. Loan licences.—(1) Applications for the grant or renewal of loan licences for the manufacture for sale 2[or for distribution] of drugs specified in Schedules C and C(1) 3[excluding those specified in Part XB and Schedule X] shall be made in Form 27A to the licensing authority and 4[shall be made upto ten items for each category of drugs categorised in Schedule M and Schedule MIII and shall be accompanied by a licence fee of rupees six thousand and an inspection fee of rupees one thousand and five hundred for every inspection or for the purpose of renewal of licences]:5[Provided that if the applicant applies for the renewal of a licence after its expiry but within six months of such expiry the fee payable for renewal of the licence shall be rupees 4[rupees six thousand and an inspection fee of rupees one thousand and five hundred plus an additional fee at the rate of rupees one thousand] per month or a part thereof.]Explanation.—For the purpose of this rule a loan licence means a licence which a licensing authority may issue to an applicant who does not have his own arrangements for manufacture but who intends to avail himself of the manufacturing facilities owned by another licensee in Form 28.(2) The licensing authority, shall, before the grant of a loan licence, satisfy himself that the manufacturing unit has adequate equipment, staff, capacity for manufacture and facilities for testing, to undertake the manufacture on behalf of the applicant for a loan licence.6[(3) Subject to the provisions of sub rule (2), the application for manufacture of more than ten items of each category of drugs on a loan licence, shall be accompanied by an additional fee at the rate of rupees three hundred for each additional item of drugs.(4) If the licensing authority is satisfied that a loan licence is defaced, damaged or lost, he may, on payment of a fee of rupees one thousand, issue a duplicate copy of loan licence.]76A. Form of loan licence to manufacture for sale 2[or for distribution of] drugs specified in Schedules C and C(1) 3[excluding the drugs specified in Schedule X] and conditions for the grant or renewal of such licence.—A loan licence to manufacture for sale 4[or for distribution of] drugs specified in Schedules C and C (1) 5[excluding the drugs specified in Schedule X] shall be issued in Form 28A, and the applicant shall, while applying for a licence to manufacture patent or proprietary medicines, furnish to the Licensing Authority evidence and data justifying that the patent or proprietary medicines—(i) contain the constituent ingredients in therapeutic/prophylactic quantities as determined in relation to the claims or conditions for which the medicines are recommended for use or claimed to be useful;(ii) are safe for use in the context of the vehicles, excipients, additives and pharmaceutical aids used in the formulations and under the conditions in which the formulations for administration and use are recommended;(iii) are stable under the conditions of storage recommended; and(iv) contain such ingredients and in such quantities for which there is therapeutic justification.]1[83A. Certificate of renewal of a loan licence.—The certificate of renewal of a loan licence in Form 28A shall be issued in Form 26A.]295 [ 83AA Duration of loan licence. —An original loan license in Form 28A or renewed loan licence in Form 26A, unless sooner suspended or cancelled, shall be 296 [valid for a period of five years on and from the date on which] it is granted or renewed:297 [Provided that if the application for the renewal of licence is made before its expiry, or if the application is made within six months of its expiry, after payment of the additional fee, the licence shall continue to be in force until orders are passed on the application and the licence shall be deemed to have expired if the application for its renewal is not made within six months of its expiry.]]138A. Application for loan licence to manufacture cosmetics.—(1) Application for grant or renewal of a loan licence for the manufacture for sale of cosmetics 2[shall be made up to ten items of each category of cosmetics categorised in Schedule MII in Form 31A to the Licensing Authority and shall be accompanied by a licence fee of rupees two thousand and five hundred and an inspection fee of rupees one thousand for every inspection thereof].Explanation.—For the purpose of this rule a ‘loan licence’ means a licence which a licensing authority may issue to an applicant who does not have his own arrangements for manufacture but who intends to avail himself of the manufacturing facilities owned by a licensee in Form 32.(2) If a person applies for the renewal of a loan licence after its expiry but within six months of such expiry, the fee payable for the renewal of such a licence shall be 2[rupees two thosuand and five hundred plus an additional fee at the rate of rupees four hundred for each month or part thereof].(3) The licensing authority shall, before the grant of a loan licence, satisfy himself that the manufacturing unit has adequate equipment, staff, capacity for manufacture and facilities to undertake the manufacture on behalf of the applicant for a loan licence.(4) The loan licence shall be granted by the licensing authority to only such applicants who propose to avail of the facilities of manufacture of cosmetics in the premises of a manufacturer located in the same State where the applicant is located. In case the manufacture of cosmetics involves any special process of manufacture or use of equipments which are not available in the State where the applicant is located, the licensing authority, after consulting the licensing authority where the manufacturing unit is located, may grant the loan licence.(5) Subject to the provisions of sub-rule (2), application for manufacture of additional items on a loan licence shall be accompanied by a fee of 2[rupees one hundred for each item subject to a maximum of rupees three thousand per application].(6) A 2[fee of rupees two hundred and fifty] shall be paid for a duplicate copy of a licence issued under sub-rule (1) if the original is defaced, damaged or lost.]1[139B. Form of loan licence to manufacture cosmetics for sale 1[or for distribution].—A loan licence to manufacture cosmetics for sale 2[or for distribution] against application in form 31A shall be granted in Form 30A.]1[141A. Certificate of renewal of loan licence.—the certificate of renewal of a licence in Form 32A shall be issued in Form 33A.]1[141AA. Duration of a loan licence.—An original loan licence in Form 32A or a renewed loan licence in Form 33A, unless sooner suspended or cancelled, shall be 2[valid for a period of five years on and from the date on which] in which it is granted or renewed:Provided that if the application for the renewal of a licence is made before its expiry, or if the application is made within six months of its expiry after payment of the additional fee, the licence shall continue to be in force until orders are passed on the application. The licence shall be deemed to have expired if the application for its renewal is not made within six months of its expiry.]1[153A. Loan Licence.—(i) An application for the grant or renewal of a loan licence to manufacture for sale of any Ayurvedic (including Siddha) or Unani drugs shall be made in Form 25E to the licensing authority along with 2[a fee of rupees six hundred].Explanation.—For the purpose of this rule, a loan licence means a licence which a licensing authority may issue to an applicant who does not have his own arrangements for manufacture but intends to avail himself of the manufacturing facilities owned by a licensee in Form 25D:Provided that in the case of renewal the applicant may apply for the renewal of the licence before its expiry or within one month of such expiry:Provided further that the applicant may apply for renewal after the expiry of one month, but within three months of such expiry in which case 3[the fee payable for renewal of such licence be rupees six hundred plus an additional fee of rupees three hundred].(ii) 4[A fee of rupees one hundred and fifty] shall be payable for a duplicate copy of a licence issued under this rule, if the original licence is defaced, damaged or lost.]1[154A. Form of loan licence to manufacture for sale Ayurvedic (including Siddha) or Unani drugs.—(1) A loan licence to manufacture for sale any Ayurvedic (including Siddha) or Unani drugs shall be issued in Form 25E.(2) A licence under this rule shall be granted by the licensing authority after consulting such expert in Ayurvedic (including Siddha) or Unani systems of medicine, as the case may be, which the State Government may approve in this behalf.(3) The licensing authority shall, before the grant of a loan licence, satisfy himself that the manufacturing unit has adequate equipment, staff, capacity for manufacture and facilities for testing, to undertake the manufacture on behalf of the applicant for a loan licence.]1[155A. Certificate of renewal of a loan licence.—The certificate of renewal of a loan licence in Form 25E shall be issued in Form 26E.]1[156A. Duration of loan licence.—An original loan licence in Form 25E or renewed loan licence in Form 26E, unless sooner suspended or cancelled, shall be 2[valid for a period of three years from the date of its issue]:Provided that if the application for the renewal of a loan licence is made in accordance with rule 153A, the loan licence shall continue to be in force until orders are passed on the application. The licence shall be deemed to have expired, if application for its renewal is not made within three month of its expiry.]1[158A. Conditions of loan licence.—A licence in Form 25E shall be subject to the following further conditions, namely:—(a) The licence in Form 25E shall be deemed to be cancelled or suspended, if the licence owned by the licensee in Form 25D whose manufacturing facilities have been availed of by the licensee is cancelled or suspended, as the case may be, under these rules.(b) The licensee shall comply with the provisions of the Act and of the rules and with such further requirements if any, as may be specified in any rules subsequently made under Chapter IVA of the Act,provided that where such further requirements are specified in the rules, these would come into force four months after publication in the Official Gazette.(c) The licensee shall maintain proper records of the details of manufacture and of the tests, if any, carried out by him, or any other person on his behalf, the raw materials and finished products.(d) The licensee shall allow an Inspector appointed under the Act to inspect all registers and records maintained under these rules and shall supply to the Inspector such information as he may require for the purpose of ascertaining whether the provisions of the Act and the rules have been observed.]2[(e) The licensee shall maintain as Inspection Book in Form 35 to enable an Inspector to record his impressions and the defects noticed.]___________1[SCHEDULE M (See rules 71, 74, 76, and 78)GOOD MANUFACTURING PRACTICES AND REQUIREMENTS OF PREMISES, PLANT AND EQUIPMENT FOR PHARMACEUTICAL PRODUCTS29.9 Loan licence manufacture and licensee (a) description of the way in which compliance of Good Manufacturing Practices by the loan licensee shall be assessed.______________________________________Guidelines For Grant Of Additional Products Permissions Under The Licence In Form-25 & FORM-28.STEP-IThe following Documents/Details To Be Submitted:1. Covering letter Addressed to the Drugs Controller and Licencing Authority for the State of Karnataka (or other state) duly signed by the applicant viz Proprietor/Partners/Managing Director/Authorized Signatory[The covering letter is an important part of the application and should clearly specify the intent of the application. The list of documents that are being submitted (Index with page number) as well as any other important and relevant information may be provided in the covering letter The covering letter should be duly signed and stamped the authorized signatory, indicating the name & designation of the authorized signatory in original issued by the Director/Company]2. Duly filled additional product proforma duly signed by the licensee viz Proprietor/Partner/Managing Director/Authorised Signatory.3 FeesFees of Rs. 300/- (for each additional product) has to be paid through challan at Government Treasury, State Bank of Mysore (or relevant other Bank for other state) under the Head of Account ‘0210 Medical and Public Health-04 Public Health-104 Fees, Fines etc.-02 Drugs and Cosmetics Act and Rules/Drugs Control Department’4 Attested true copy of the valid manufacturing licence(s).5 Declaration regarding the manufacturing facility and approved CTS for the proposed dosage form.6 Photocopy of DCG (I) permission/NOC in case of new drug.7 Photocopy of export order, rate contract order if the proposed products are required to be supplied against specific order.8 List of product/s to be manufactured In triplicate, with declaration duly signed.DownLoad Format of Declaration9 Copy of the specimen label duly signed by licencee.10 Standards & analytical procedure of each product for the patent and proprietary drugs proposed (quote the relevant authoritative books followed).11 Detail formula, shelf life, details of parallel products and packing specifications for each product.12 Details of the following:(a) Stability studies conducted and the justification for the shelf life period assigned under the conditions of storage recommended.(b) Therapeutic justification for each constituent in the product in relation to the claims made or the product is recommended for use, in case of Patent and Proprietary Medicines. (c) safety declaration as required under Rule 71(6), 71-B, 76(7), 76-A as applicable of Drugs & Cosmetics Rules depending upon the product for P & P medicines as applicable.DownLoad Safety Declaration13 Flow sheet in the case of Bulk Drugs along with the details like in process controls employed during the manufacture,14 Chemical reactions involved in the synthesis of Bulk Drug and Brief Method of Manufacture.15 Brand name declaration in the format specified duly signed by the licencee.DownLoad Brand name declaration16 Copy of the test licence in form 29 and product development data of the trial batches.17 Standards, and method of analysis of active/excipients which are not official in any pharmacopoeia.18 In case of proposed products intended to be manufactured in Principle-to-Principle basis, the photocopy of the agreement supported with trademark registration document and the copy of the whole sale Drug licence of the Third party.19 Photocopy of official monographs for the proposed product/s and its active ingredient and excipients.Download Additional Information FormNote* The above documents shall be serially numbered and to be submitted as per the sequence mentioned above.** The above requirements are not exhaustive one. In case of products of special nature/category, additional documents/ clarifications is required to be submitted whenever called for.STEP-IIThe application is verified by the manufacturing section for the correctness of the list of documents submitted and is then processed and forwarded to concerned Drugs inspector/Assistant Drugs Controller (HQ) for scrutiny and if the submitted documents are in order the application is forwarded to Drugs controller and licensing Authority through Deputy Drugs Controller (HQ) and Additional Drugs Controller for orders for the Grant of permission.STEP-IIIIf the submitted application & information is not in order or requires any clarifications a compliance letter will be served to the applicant at the level of Deputy Drugs Controller only.STEP-IVIf all documents / conditions / requirements as prescribed under the Drugs and Cosmetics Act and Rules there under and any specific office orders are complied, it is recommended by the concerned officer for grant of permission to manufacture additional product/s under the valid licence through proper channel as per the administrative order of Drugs Controller, additional product/s permission will be granted by Licensing Authority.

The information and Forms relating to issue of various licenses under various Rules framed under Tamil Nadu Prohibition Act, 1937 are furnished below.SL Category Licensing authority Purpose Rule1. DL1 Government For the wholesale vend of Denatured Spirit Tamil Nadu Denatured Spirit Methyl Alcohol & Varnish(French Polish) Rules,19592. DL2 CPE For possession and use of Denatured Spirit/Methyl Alcohol(Methanol) in the manufacture of specified commodities other than Varnish -do-3. ML2 Collector For the possession and sale of Molasses Tamil Nadu Molasses Control and Regulation Rules,19584. ML4 DRO For the possession and use of Molasses -do-5 ML5 Collector Licence for Import / Export of Molasses -do-6 ML6 Collector Permit for transport of Molasses within state -do- 7. Distillery Licence CPE (Prior approval of the Govt.) For the grant of privilege and licence to establish a Distillery and manufacture spirit therein Tamil Nadu Distillery Rules,1981[Rule 5(a) and 5(b)] 8. RL1 Collector (Exceeding 50 litres, after getting prior approval of the Govt.) For possession and sale of Rectified Spirit/Absolute Alcohol Tamil Nadu Rectified Spirit Rules,2000 (Rule3(1) and 5(1)) 9. RL2 -do- For possession and sale of Rectified Spirit/absolute alcohol for bonafide chemical purposes for bonafide dispensary, scientific, educational, research and laboratory purposes -do- (Rule 3(2) 10. RL3 CPE For possession and use of Rectified Spirit/Neutral Spirit for the manufacture of Indian Made Foreign Spirit products by the holders of licences under Tamil Nadu Indian Made Foreign Spirit (Manufacture) Rules,1981 and for possession use of Rectified Spirit by the licence holders under the Medicinal and Toilet Preparations (Excise Duties) Rules,1956 and the EL1 licence holders under the Tamil Nadu Spirituous Essence Rules,1972 (Rlules3(1), 4(2)&5(2) -do- 11. RL4 CPE For possession and use of Rectified Spirit/Absolute Alcohol for Industrial (ie)non-potable purposes and other purposes except the purposes covered under RL2 and RL3 licences Tamil Nadu Rectified Spirit Rules,2000 12. Indian Made Foreign Spirit Licence CPE with the prior approval of the Govt. For Manufacture of Indian Made Foreign Spirit The Tamil Nadu Indian Made Foreign Spirit (Manufacture) Rules,1981 13. Brewery Licence CPE For Manufacture of Beer The Tamil Nadu Brewery Rules,1983 14. Mass Wine CPE For Manufacture of Mass Wine Tamil Nadu Mass Wine Rules,1984 15 Liquor Retail Vending in Shops and Bars CPE As per Rule 3(1) of Tamil Nadu Liquor Retail Vending (Shops and Bars) Rules,2003. Retail sale of bottled Indian Made ForeignSpirit, in shops and bars by the TASMAC for the whole State of the Tamil Nadu. Tamil Nadu Liquor Retail Vending(in shops and Bars) Rules,2003. 16 Sale of IMFS by wholesale CPE Sale of IMFS by wholesale through TASMAC main Depot , Branch Depots Tamil Nadu Indian Made Foreign Spirits (Supply by WholeSale) Rules, 1983. 17 FL2 CPE Licence for possession of liquor by a non-proprietary club for supply to Members Tamil Nadu Liquor(Licence and Permit Rules,1981 18 FL3 CPE Licence for possession of liquor by the Star Hotels for supply to foreign tourists and foreigners resident in India holding personal permits and also citizens of India holding personal permits for consumption within the licensed ;room of the Hotel or for renewal to their private rooms in the same Hotel in which they stay for consumption. -do- 19 FL-3A CPE Licence for possession of Liquor by hotel run by the Tamil Nadu Tourism Development Corporation for supply to persons who actually stay in the Hotel for a minimum period of 3 hours for consumption in the room of the hotel. -do- 20 FL-3AA CPE Licence for possession of liquor by a hotel run by the Franchisee of the Tamil Nadu Tourism Development Corporation for supply to persons, who actually stay in the hotel for a minimum period of three hours for consumption in the licensed rooms of the hotel or in their private rooms in which they actually stay or in the lawns and the appurtenants of that hotels. -do- 21 FL4 CPE Licence for possession for liquor by the Manager, Canteen Stores Department (India), Canteen Retail and Bulk issue Depot, Fort St. George, (Chennai) for supply to military contractors and officers of the military units holding licences in Form F.L.4 (A) 2(and for export to the Andaman and Nicobar Islands for the unit-run canteens of the Armed Forces stationed in the said Islands.) -do- 22 FL-4A Collector For possession and supply of liquor to Military units Military Personnels and Ex-Servicemen. -do- 23 FL5 Collector For possession and issue of liquor by the Chennai Seamen’s Institute / Chennai Seamen’s Hostel to the officers or Seamen of the Merchant Navy. -do- 24 FL6 Collector For possession and use of liquor for Scientific, Industrial or such like purposes -do- 25 FL7 Collector For possession and supply of wine or grape juice or other such liquor for sacramental purposes. -do- 26 FL8 CPE Special licence for possession and issue of liquor to International Passengers on board in the Aircraft of Air-India. -do- 27 FL9 CPE Special Licence for possession and issue of liquor including bottled Liquor to International Air Passengers transiting the Meenambakkam Civil Air Port who are required to wait at the Airport transit lounge reserved for such passengers before resuming their journeys (and issue of foreign liquor to the foreign diplomats stationed at (Chennai). -do- 28 FL10 CPE Special Licence for possession of liquor by an approved restaurant and to serve liquor for approved restaurant and to serve liquor for consumption in the bar of the restaurant to the foreign tourists or foreign residents of India or Indian Citizens during their halt at the airport. -do- 29 FL-11 CPE Licence to enable the TASMAC Ltd. to sell foreign liquor by retail. -do- 30 L1 CPE Licence to manufacture Medicinal and Toilet Preparations containing alcohol, opium, Indian hemp and other Narcotic drugs and narcotics under bond for payment of duty. Medicinal and Toilet Preparations(Excise Duty) Rules,1956 31 L2 Collector Licence to manufacture Medicinal and Toilet Preparations containing alcohol, Opium, Indian hemp and other Narcotic drug and Narcotics outside bond -do- 32 L3 Collector Licence for Ayurvedic or Unani practitioner to manufacture Ayurvedic or Unani preparations containing Self generated alcohol for dispensing and not for trade purposes. -do- 33 L4 Collector Licence for a Bonded Ware house -do- 34 SPXI Collector Wholesale licence in Form SP XI for the possession and sale of Spirituous preparations. Tamil Nadu Spirituous Preparations (Control) Rules, 1984 35 SP XIV Collector Retail licence in Form SP XIV for the possession and sale of Spirituous preparations. -do- 36 G.E.P. under SPXI and SPXIV CPE To Export Restricted Preparations to outside to State. -do- 37 I.P. under SPXI and SPXIV CPE To Import any Restricted Preparations. -do- 38 NDRC Collector To possess and sell medicines containing any manufactured drugs (Narcotic Drugs) Tamil Nadu Narcotic Drugs Rules, 1985 39 I.P. under NDRC CPE To Import manufactured drugs (Narcotic Drugs) -do- 40 E.P. under NDRC CPE To Export manufactured Drugs (Narcotic Drugs) -do- 41 E.L.1. Commissioner. For the manufacture of essences Tamilnadu Spirituous Essences Rules 1972 42 E.L.2 Collector For wholesale vend of essence -do- 43 E.L.3 Collector For retail sale of essences -do- 44 E.L.4 Collector For possession and use of essences -do- 45 Wine Manufact-uring Commissioner For Manufacture of Wine Tamilnadu Wine (Manufacture) Rules, 2006 . 46 The Tamilnadu Disposal of Articles (Confiscated Under the Tamilnadu Prohibition act) Rules, 1979 47 The Tamilnadu Liquor (Transit) Rules, 1982