US Codex
C.F.R.
Legal Codes
United States Code
U.S.C.
Federal statutory law
Code of Federal Regulations
C.F.R.
Federal administrative regulations (eCFR)
Browse by date
View an earlier version
Go
Latest
Current
Browse all versions by date
Notes
Notes
Browse by date
Home
About
Privacy
MCP
…
/
Code of Federal Regulations
/
Title 21
/
Chapter I — Food and Drug Administration, Department of Health and Human Services
/
Subchapter D — Drugs for Human Use
/
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
›
Add note
Incoming references
Copy permalink
Cite
Cite this provision
×
Format
Bluebook
ALWD
APA
MLA
Include provision text
Copy citation
Incoming references
×
Open in new tab
✕