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Code of Federal Regulations
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Title 21
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Chapter I — Food and Drug Administration, Department of Health and Human Services
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Subchapter D — Drugs for Human Use
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Part 320 — Bioavailability and Bioequivalence Requirements
‹
Pt. 317
Qualifying Pathogens
Pt. 328
Over-The-Counter Drug Products Intended for Oral Ingestion That Contain Alcohol
›
Part 320 — Bioavailability and Bioequivalence Requirements
Search Part 320 full text →
Subpt. A
General Provisions
§320.1
Subpt. B
Procedures for Determining the Bioavailability or Bioequivalence of Drug Products
§§320.21 to 320.63
‹
Pt. 317
Qualifying Pathogens
Pt. 328
Over-The-Counter Drug Products Intended for Oral Ingestion That Contain Alcohol
›
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