Schedules: All types of Drugs

Schedules: All types of Drugs under Drugs and Cosmetics Act 1940 and Rules 1945

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Last Updated on June 15, 2021 by The Health Master

Schedules –All types of Drugs under Drugs and Cosmetics Act 1940 and Rules 1945

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As per Drugs and Cosmetics Act 1940 and Rules 1945 we have provided some important Schedules for drugs relevant to the above said topic, Click below links for more information:

Schedule-B: Fees for test or analysis by the Central Drugs Laboratories or State Drugs Laboratories
Schedule-B

Schedule-C-C1: Biological and special products
Schedule-C-C1

Schedule-D: Class of drugs and Extent and conditions of exemption
Schedule-D

Schedule-D1: Information and undertaking required to be submitted by the manufacturer or his authorized agent with the Application Form for a Registration Certificate
Schedule-D1

Schedule-DII: Information required to be submitted by the manufacturer or his authorized agent with the Application Form for the registration of a bulk drug / formulation / special product for its import into India
Schedule-D-II

Schedule-G: List of drugs falls under Schedule-G
Schedule-G

Schedule-H: List of drugs falls under Schedule-H
Schedule-H

Schedule-H1: List of drugs falls under Schedule H1
Schedule-H1

Schedule-K: Class of drugs and Extent and Conditions of Exemption
Schedule-K

Schedule-L1: (GLP) Good laboratory practices and requirements of premises and equipment
Schedule-L1

Schedule-M: (GMP) Good manufacturing practices for premises and materials
Schedule-M

Schedule-O: Provisions applicable to Black Fluids and White Fluids
Schedule-O

Schedule-P: Storage conditions of drugs
Schedule-P

Schedule-P1: Pack size of drugs
Schedule-P1

Schedule-T: (GMP) Good manufacturing practices for Ayurvedic, Siddha and Unani medicines
Schedule-T

Schedule-T-A: Form for record of utilizaion of raw material by Ayurveda or Siddha or Unani licensed manufacturing units during the financial year
Schedule-T-A

Schedule-X: List of drugs falls under Schedule-X
Schedule-X

Schedule-Y: Requirements and guidelines for permission to import and / or manufacture of new drugs for sale or to undertake clinical trials
Schedule-Y


Compiled by:
Rakesh DahiyaSDCO cum Licensing Authority, FDA Haryana

Schedules: Cosmetics

Schedules: Medical Devices

Schedules: Clinical Trials

Licensing procedure for manufacturing of Drugs

Latest Notifications: D&C Rules 1945

Latest Notifications: D&C Act 1940

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