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⚖️ Pharmaceutical Jurisprudence Complete Guide
A comprehensive reference guide covering all statutory schedules under the Drugs and Cosmetics Rules 1945, Pharmacy Act 1948, and essential drug control acts frequently tested in Drug Inspector and Pharmacist recruitment exams.
Complete Reference Table: All Schedules Under D&C Rules, 1945
| Schedule | Statutory Subject Matter & Requirements |
|---|---|
| Schedule A | List of statutory forms for application, grant of licenses, certificates, and analysis reports. |
| Schedule B | Fees payable for analysis and test by the Central Drugs Laboratory (CDL) or Government Analysts. |
| Schedule C & C1 | Special biological and other products (sera, vaccines, toxins, antigens, antibiotics, ophthalmic solutions). |
| Schedule D | List of substances and classes of drugs exempted from provisions of import of drugs. |
| Schedule F (Part XII-B) | Requirements for the functioning and licensing of a Blood Bank. |
| Schedule G | List of substances required to be used strictly under medical supervision (e.g., Metformin, Bleomycin). |
| Schedule H | Prescription drugs that can be sold by retail only on the prescription of a Registered Medical Practitioner (RMP). |
| Schedule H1 | Certain 3rd/4th gen antibiotics, anti-TB drugs, and habit-forming drugs; requires separate register for 3 years. |
| Schedule M | Good Manufacturing Practices (GMP) and factory premises requirements. |
| Schedule M1 | Good Manufacturing Practices for Homeopathic medicines. |
| Schedule N | List of minimum equipment and apparatus required for efficient running of a retail pharmacy. |
| Schedule P | Life periods (shelf-life / expiry dates) and storage conditions for individual drugs. |
| Schedule X | Special psychotropic and habit-forming substances (e.g., Ketamine, Amphetamines); strict dual prescription retention. |
| Schedule Y | Requirements and guidelines for permission to import and/or manufacture of new drugs for clinical trials. |
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