21 Food and Drugs 4 2007-04-01 2007-04-01 false Table Of Contents Food and Drugs FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED) CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)

(Parts 200 to 299)

 Editorial Note:

Nomenclature changes to chapter I appear at 59 FR 14366, Mar. 28, 1994, and 66 FR 56035, Nov. 6, 2001.

 SUBCHAPTER C—DRUGS: GENERAL Part Page 200 General 5 201 Labeling 8 202 Prescription drug advertising 91 203 Prescription drug marketing 100 205 Guidelines for State licensing of wholesale prescription drug distributors 112 206 Imprinting of solid oral dosage form drug products for human use 117 207 Registration of producers of drugs and listing of drugs in commercial distribution 118 208 Medication Guides for prescription drug products 129 210 Current good manufacturing practice in manufacturing, processing, packing, or holding of drugs; general 132 211 Current good manufacturing practice for finished pharmaceuticals 135 216 Pharmacy compounding 155 225 Current good manufacturing practice for medicated feeds 156 226 Current good manufacturing practice for Type A medicated articles 163 250 Special requirements for specific human drugs 168 290 Controlled drugs 176 299 Drugs; official names and established names 177