CFR - Code of Federal Regulations Title 21

The information on this page is current as of Dec 22, 2023.

For the most up-to-date version of CFR Title 21, go to the Electronic Code of Federal Regulations (eCFR).

TITLE 21--FOOD AND DRUGS
CHAPTER I--FOOD AND DRUG ADMINISTRATION
DEPARTMENT OF HEALTH AND HUMAN SERVICES
SUBCHAPTER C - DRUGS: GENERAL

PART 250 SPECIAL REQUIREMENTS FOR SPECIFIC HUMAN DRUGS

Subpart A - Drugs Regarded as Misbranded
   § 250.11 - Thyroid-containing drug preparations intended for treatment of obesity in humans.
   § 250.12 - Stramonium preparations labeled with directions for use in self-medication regarded as misbranded.

Subpart B - New Drug or Prescription Status of Specific Drugs
   § 250.100 - Amyl nitrite inhalant as a prescription drug for human use.
   § 250.101 - Amphetamine and methamphetamine inhalers regarded as prescription drugs.
   § 250.102 - Drug preparations intended for human use containing certain "coronary vasodilators".
   § 250.103-250.104 - [Reserved]
   § 250.105 - Gelsemium-containing preparations regarded as prescription drugs.
   § 250.106-250.107 - [Reserved]
   § 250.108 - Potassium permanganate preparations as prescription drugs.

Subpart C - Requirements for Drugs and Foods
   § 250.201 - Preparations for the treatment of pernicious anemia.

Subpart D - Requirements for Drugs and Cosmetics
   § 250.250 - Hexachlorophene, as a component of drug and cosmetic products.

Authority: 21 U.S.C. 321, 336, 342, 352, 353, 355, 361(a), 362(a) and (c), 371, 375(b).
Source: 40 FR 14033, Mar. 27, 1975, unless otherwise noted.