1. LawStack
  2. Title 21 - Food and Drugs
  3. Chapter I - FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
  4. Subchapter C - DRUGS: GENERAL
  5. Part 211 - CURRENT GOOD MANUFACTURING PRACTICE FOR FINISHED PHARMACEUTICALS
  6. 21 CFR Subpart G
21 CFR Subpart G
Packaging and Labeling Control
June 25, 2020
§
211.122
Materials examination and usage criteria
§
211.125
Labeling issuance
§
211.130
Packaging and labeling operations
§
211.132
Tamper-evident packaging requirements for over-the-counter (OTC) human drug products
§
211.134
Drug product inspection
§
211.137
Expiration dating
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Subpart E Control of Components and Drug Product Containers and Closures
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Subpart H Holding and Distribution

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