Domiyance Finance Consultancy LLP

Drug License Apply Online

The government has stringent rules for granting licenses for the manufacturing and selling of drugs and medicine. The Act that governs the end to end process from manufacture to the sale of drugs in India is the Drugs and Cosmetics Act, 1940. We help to file wholesale or retail drug license applications anywhere in India.

Pricing for Wholesale or Retail Drug License

Fssai Registration

₹ 2,999/-

Required if the turnover is less than 12 lac in a Financial Year & the business is within the state

Fssai State License

₹8,499/-

When turnover is more than 12 Lac & upto 20 Crores for retailer/ 30 Crores for wholesalers

Fssai Central License

₹ 11,999/-

For all cases where turnover exceeds limits prescribed for state License or involved in export.

Basic Overview of Drugs or Pharmaceutical Business

Ensuring everyone has equal and fair access to drugs and medicine is the primary concern of any government. But the right to manufacture and sell drugs and medicines has to be given cautiously.

Section 3(b) of the Drugs and Cosmetics Act,1940 defines “drug” to include all medicines and devices for the use of human beings or animals internally or externally, and all substances planned to be used for or in the diagnosis, mitigation, treatment, or prevention of any disorder or disease in animals or human beings, including preparations applied on the human body for the purpose of repelling insects like mosquitoes; it also includes all substances that can be used for the destruction of insects and all components of a drug – like empty gelatin capsules. The definition was amended in 1964, to include Ayurvedic and Unani Drugs.

The competent authority grants a drug license under the Drugs and Cosmetic Act of 1940 to carry out a business concerning drugs/medicines or cosmetics. In other words, no person can start or carry out a business dealing with drugs or cosmetics in India without a licence from the concerned authority. All types of drugs or cosmetics business fall under the Drugs and Cosmetics Act, 1940, including allopathic, homoeopathic, ayurvedic or unani drugs.

Purpose of Drug Licence

The access to medicines and drugs must be restricted and regulated to ensure that such goods are not abused or misused by individuals. Thus, all pharmacists, wholesalers, retailers, manufacturers, sellers, dealers and importers of drugs, cosmetics, ayurvedic, Siddha and Unani drugs have to mandatorily obtain drug license under the Drugs and Cosmetics Act, 1940.

The purpose of the drug license is to grant permission to allow enterprises or individuals to engage in businesses related to drugs and cosmetics. No enterprise or individual can operate a business dealing in drugs, medicines or cosmetics without obtaining a drug license in India.

The Drugs and Cosmetics Act, 1940 and the Drugs and Cosmetics Rules, 1945, help the government regulate and monitor the quality of drugs sold in India. The government exercises control over drugs from the raw material stage during manufacture, sale, distribution and till it is sold on to a patient or consumer by a pharmacist in a retail pharmacy, hospital or dispensary.

The government also exercises control in the aspects related to import and export of medicines, sale of the drug to a minor, consumption of schedule H & X drugs, etc., that requires thorough monitoring and cautious execution. The drug license is granted by the drug controlling authority under the Drugs and Cosmetics Act, 1940.

Types of Drug License

Looking at the definition of “drug”, the pharmaceutical business in India requires the following types of licenses:

  • Manufacturing License– License issued to a business that manufactures drugs inclusive of allopathic/homoeopathy medicines.
  • Sale License – License issued for the sale of drugs. It has the following bifurcations: Wholesale Drug License; Retail Drug License
  • Wholesale License – A drug wholesaler must obtain a wholesale licence. Wholesale means the sale of the drug to a person/retailer to further sell it.
  • Retail License – A retail license is required for the retail sale of drugs. A retail sale means the sale of drugs or cosmetics for the consumption of the end consumer. Retailers can sell it to a dispensary, hospital, educational, medical, or research institute. Retailers engaged in pharmaceuticals, cosmetics, stand-alone pharmacists, ayurvedic shops, etc need this license.
  • Loan License – License issued to a business that does not own the manufacturing unit but uses the manufacturing facilities of another licensee.
  • Import License – License is issued to any dealer importing the products for the manufacturing of drugs or is engaged in the business of importing drugs in India.
  • Multi-Drug License – License issued to businesses that own pharmacies in multiple states with the same name.

list of documents

The documents essential for obtaining a sale license are:

  • Constitution of the entity, Memorandum of Association (MOA), Articles of Association (AOA) for a company, partnership deed, LLP agreement in case of partnership and LLP;
  • ID proof of partner/director/proprietor;
  • Documents related to premises – Copy of ownership documents of property or rental agreement and NOC from the owner of the rented premises as the case may be;
  • Site plan and key plan of the premises;
  • Copy of Board resolution permitting obtaining of a license;
  • Proof of availability of storage space as cold storage, refrigerator, etc;
  • Copy of challan as proof of depositing fee;
  • Affidavit regarding non-conviction of proprietor/partner/director and the firm;
  • The affidavit from the registered pharmacist/competent person;
  • Cover letter with name and designation of the applicant;
  • Declaration form in a prescribed format;
  • Applicant’s qualification certificate;
  • For a pharmacist at a retail sale:
    • Proof of qualification;
    • Registration of local pharmacy council;
    • Appointment letter;
  • For a pharmacist at a wholesale sale:
    • Proof of qualification;
    • Experience certificate;
    • Appointment letter.

Step wise procedure

The drug controlling authority or the regulatory authority is responsible for issuing the drug license. The applicant must apply to the respective drug controlling authority based on the license he/she requires as each drug controlling authority is responsible to issue different licenses (as stated above). The following is the process for obtaining the drug license:

Visit the respective drug controlling authority website

The applicant must visit the respective drug controlling authority (SDSCO, CDSCO or Ayush) depending on the type of license he/she is applying for since each drug controlling authority is responsible for the issue of different types of drug licenses.

Filing of application

The applicant must file the drug license application online on the respective drug controlling authority website. The applicant must fill all the details asked in the application form.

Upload documents

After filling in the details on the application form, the next step is to upload the documents and submit the form along with the applicable fees. The applicant must keep all the documents updated before filing the application.

Visit by drug inspector

After receiving the application form, the drug Inspector will personally visit the company premises, shop or the drugstore for the verification of documents and correctness of facts stated in the application.

Grant of the drug license

After inspection and verification by the drug inspector, the drugs controller will issue the drug license.

Prerequisites For Obtaining a License