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
2026-08-27
Browse all versions by date
Notes
Notes
Browse by date
About
Privacy
MCP
…
/
Code of Federal Regulations
/
Title 21
/
Chapter I — Food and Drug Administration, Department of Health and Human Services
/
Subchapter C — Drugs: General
/
Part 208 — Medication Guides for Prescription Drug Products
‹
Pt. 207
Requirements for Foreign and Domestic Establishment Registration and Listing for Human Drugs, Including Drugs That Are Regulated under a Biologics License Application, and Animal Drugs, and the National Drug Code
Pt. 209
Requirement for Authorized Dispensers and Pharmacies to Distribute a Side Effects Statement
›
Part 208 — Medication Guides for Prescription Drug Products
Search Part 208 full text →
Subpt. A
General Provisions
§§208.1 to 208.3
Subpt. B
General Requirements for a Medication Guide
§§208.20 to 208.26
‹
Pt. 207
Requirements for Foreign and Domestic Establishment Registration and Listing for Human Drugs, Including Drugs That Are Regulated under a Biologics License Application, and Animal Drugs, and the National Drug Code
Pt. 209
Requirement for Authorized Dispensers and Pharmacies to Distribute a Side Effects Statement
›
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
✕