DRUG LICENSE

All companies engaged in the distribution of pharmaceutical supplements and medicines must have a drug license, commonly known as a pharmaceutical license. The Drugs & Cosmetics Act, 1940 states in Section 3(b) that "drugs" include all devices and medications for internal or external use in both humans and animals, as well as all substances proposed for use in the mitigation, treatment, diagnosis, or prevention of any disorder or disease in humans or animals. Ayurvedic and Unani drugs are now included in the definition, which was changed in 1964. To conduct business in India's pharmaceutical and cosmetic industries, a drug license is required. The Drugs & Cosmetics Act, 1940, which applies to all of India, contains a provision for this.

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ABOUT

Drug License Registration is location-specific. It means if the drugs are stocked or sold for sale and distribution at more than one place, then the application shall be made to every state, and a license shall be issued regarding each such place except for migrant vendors. Drug license acts as an authority given by the Government of India to the owner of the drugstore or pharmacy. The Drugs and the Cosmetics Act, 1940, is the governing force for the issuance of this License in India. This act provides the provisions for carrying out the business of medicines, drugs, or cosmetics in India.

DOCUMENTS REQUIRED

Identiry Proof
Key Plans
Constitution of the Entity​
Copy of Board Resolution
NOC (No Objection Certificate)
Challan
Affidavit
Cover Letter

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