CFR 21, Parts 300 to 499, Food and Drugs, April 01, 2016 (Volume 5 of 9) Download PDF By Office of the Federal Register (CFR)

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Code of Federal Regulations Title 21, Volume 5, April 1, 2016 contains regulations governing Food and Drugs and may also be referenced as:
- Code of Federal Regulations Title 21, Volume 5, April 1, 2016
- CFR Title 21
- CFR 21, Food and Drugs
- CFR 21, Parts 300 to 499, Food and Drugs

This volume contains Parts 300 to 499:
- Part 300; GENERAL
- Part 310; NEW DRUGS
- Part 312; INVESTIGATIONAL NEW DRUG APPLICATION
- Part 314; APPLICATIONS FOR FDA APPROVAL TO MARKET A NEW DRUG
- Part 315; DIAGNOSTIC RADIOPHARMACEUTICALS
- Part 316; ORPHAN DRUGS
- Part 317; QUALIFYING PATHOGENS
- Part 320; BIOAVAILABILITY AND BIOEQUIVALENCE REQUIREMENTS
- Part 328; OVER-THE-COUNTER DRUG PRODUCTS INTENDED FOR ORAL INGESTION THAT CONTAIN ALCOHOL
- Part 329; NONPRESCRIPTION HUMAN DRUG PRODUCTS SUBJECT TO SECTION 760 OF THE FEDERAL FOOD, DRUG, AND COSMETIC ACT
- Part 330; OVER-THE-COUNTER (OTC) HUMAN DRUGS WHICH ARE GENERALLY RECOGNIZED AS SAFE AND EFFECTIVE AND NOT MISBRANDED
- Part 331; ANTACID PRODUCTS FOR OVER-THE-COUNTER (OTC) HUMAN USE
- Part 332; ANTIFLATULENT PRODUCTS FOR OVER-THE-COUNTER HUMAN.
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