FDA 21 CFR PART 200 TO 299 SUBCHAPTER C—DRUGS: GENERAL
21 CFR Part 202 Prescription Drug Advertising
21 CFR Part 203 Prescription Drug Marketing
21 CFR Part 205 Guidelines For State Licensing Of Wholesale Prescription Drug Distributors
21 CFR Part 206 Imprinting Of Solid Oral Dosage Form Drug Products For Human Use
21 CFR Part 208 Medication Guides For Prescription Drug Products
21 CFR Part 211 Current Good Manufacturing Practice For Finished Pharmaceuticals
21 CFR Part 212 Current Good Manufacturing Practice For Positron Emission Tomography Drugs
21 CFR Part 216 Human Drug Compounding
21 CFR Part 225 Current Good Manufacturing Practice For Medicated Feeds
21 CFR Part 226 Current Good Manufacturing Practice For Type A Medicated Articles
21 CFR Part 250 Special Requirements For Specific Human Drugs
21 CFR Part 251 Section 804 Importation Program