A step-by-step process to obtain a wholesale drug license for manufacturers – eligibility criteria, required document, validity and process.
The pharmacy business in India is booming. To ensure consumer safety, the Government keeps changing guidelines that aid streamlining of the processes as well. To start manufacturing drugs, the main procedure is to obtain a drug license from the respected authorities.
The Drugs and Cosmetics Act, 1940 governs obtaining the license for manufacturing drugs in India. Any person who is interested in obtaining a license from the Food Safety and Drug Administration needs to file respective forms to the State Licensing Authority.
The schedule C of the Drugs and Cosmetics Act, 1945 contains the application and licensing of wholesale drug license. The overall process of licensing requires 1 month for approval. The approval depends on the review of Drug Inspector and the report which he sends to the Licensing Authority.
The license is distributed based on the type of business, for example, retail chemist shop require Forms 20 and 21 (Allopathic) whereas ayurvedic chemist shop requires Form 20C. For the wholesale license, Form 20B and 21B should be acquired and for Schedule X drugs Form 20G is required.
A wholesale drug license is required for manufacturing pharmaceuticals, distribution, sale, or store of the medication. The license proves that you are an authorized person with an authorized business for manufacturing or distributing pharmaceuticals. Without registration, it is illegal to manufacture drugs in India.
To obtain the Wholesale drug license in India, the manufacturer has to meet the criteria given below:
Documents Filling: The applicant must have all the required documents and certifications according to the Drugs and Cosmetics Act, 1940 and Drugs and Cosmetics Rule, 1945 for successful approval of the application.
Required Documents: Following documents are required generally for processing the application:
Also Read – What Are The Benefits Of Having A Wholesale Drug License In Form 20B & 21B?
The drug license is valid perpetually until suspended by the Drug Inspector due to any reason; however, retainer fee is required to be submitted every Five years.
The wholesale drug license governs distribution and sale of pharmaceuticals in the country. It is the responsibility of the proprietor, the pharmacist and the authorized management to conduct the wholesale business as per the laid down rules and schedules. The application process is purely online and can be easily done with the required documents and certifications in place.
Saurangi is a food regulatory expert with 8 years of experience. She shares her knowledge and insights on regulatory updates, food trends, best practices, and news. Follow her for expert insights and practical advice on all things for food regulatory
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