---
kind: "unit"
title: "21"
title_heading: "Food and Drugs"
key: "chI/subchC"
level: "subchap"
label: "Subchapter C"
heading: "Drugs: General"
release: "ecfr-current"
date: "2026-08-27"
url: "https://uscodex.org/cfr/21/chI-subchC"
sections_count: 355
---

# Subchapter C — Drugs: General

Title 21 C.F.R. — Food and Drugs › Chapter I — Food and Drug Administration, Department of Health and Human Services

## Contents

- [Part 200 — General](/cfr/21/chI-subchC-part200.md)
- [Part 201 — Labeling](/cfr/21/chI-subchC-part201.md)
- [Part 202 — Prescription Drug Advertising](/cfr/21/chI-subchC-part202.md)
- [Part 203 — Prescription Drug Marketing](/cfr/21/chI-subchC-part203.md)
- [Part 205 — Guidelines for State Licensing of Wholesale Prescription Drug Distributors](/cfr/21/chI-subchC-part205.md)
- [Part 206 — Imprinting of Solid Oral Dosage Form Drug Products for Human Use](/cfr/21/chI-subchC-part206.md)
- [Part 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](/cfr/21/chI-subchC-part207.md)
- [Part 208 — Medication Guides for Prescription Drug Products](/cfr/21/chI-subchC-part208.md)
- [Part 209 — Requirement for Authorized Dispensers and Pharmacies to Distribute a Side Effects Statement](/cfr/21/chI-subchC-part209.md)
- [Part 210 — Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs; General](/cfr/21/chI-subchC-part210.md)
- [Part 211 — Current Good Manufacturing Practice for Finished Pharmaceuticals](/cfr/21/chI-subchC-part211.md)
- [Part 212 — Current Good Manufacturing Practice for Positron Emission Tomography Drugs](/cfr/21/chI-subchC-part212.md)
- [Part 213 — Current Good Manufacturing Practice for Medical Gases](/cfr/21/chI-subchC-part213.md)
- [Part 216 — Human Drug Compounding](/cfr/21/chI-subchC-part216.md)
- [Part 225 — Current Good Manufacturing Practice for Medicated Feeds](/cfr/21/chI-subchC-part225.md)
- [Part 226 — Current Good Manufacturing Practice for Type a Medicated Articles](/cfr/21/chI-subchC-part226.md)
- [Part 230 — Certification and Postmarketing Reporting for Designated Medical Gases](/cfr/21/chI-subchC-part230.md)
- [Part 250 — Special Requirements for Specific Human Drugs](/cfr/21/chI-subchC-part250.md)
- [Part 251 — Section 804 Importation Program](/cfr/21/chI-subchC-part251.md)
- [Part 290 — Controlled Drugs](/cfr/21/chI-subchC-part290.md)
- [Part 299 — Drugs; Official Names and Established Names](/cfr/21/chI-subchC-part299.md)