Drugs: General

  1. Law
  2. CFR 21
  3. Food and Drugs
  4. Food and Drug Administration, Department of Health and Human Services
  5. Drugs: General

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Part
200

General

Part
201

Labeling

Part
202

Prescription Drug Advertising

Part
203

Prescription Drug Marketing

Part
205

Guidelines for State Licensing of Wholesale Prescription Drug Distributors

Part
206

Imprinting of Solid Oral Dosage Form Drug Products for Human Use

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

Part
208

Medication Guides for Prescription Drug Products

Part
209

Requirement for Authorized Dispensers and Pharmacies to Distribute a Side Effects Statement

Part
210

Current Good Manufacturing Practice in Manufacturing, Processing, Packing, or Holding of Drugs; General

Part
211

Current Good Manufacturing Practice for Finished Pharmaceuticals

Part
212

Current Good Manufacturing Practice for Positron Emission Tomography Drugs

Part
216

Human Drug Compounding

Part
225

Current Good Manufacturing Practice for Medicated Feeds

Part
226

Current Good Manufacturing Practice for Type a Medicated Articles

Part
250

Special Requirements for Specific Human Drugs

Part
251

Section 804 Importation Program

Part
290

Controlled Drugs

Part
299

Drugs; Official Names and Established Names