Title 21

PART 216

Part 216 - Human Drug Compounding

PART 216 - HUMAN DRUG COMPOUNDING Authority:21 U.S.C. 351, 352, 353a, 353b, 355, and 371. Source:64 FR 10944, Mar. 8, 1999, unless otherwise noted.

21:4.0.1.1.13.1SUBPART A
Subpart A - General Provisions [Reserved]
21:4.0.1.1.13.2SUBPART B
Subpart B - Compounded Drug Products
21:4.0.1.1.13.2.1.1SECTION 216.23
   216.23 Bulk drug substances that can be used to compound drug products in accordance with section 503A of the Federal Food, Drug, and Cosmetic Act.
21:4.0.1.1.13.2.1.2SECTION 216.24
   216.24 Drug products withdrawn or removed from the market for reasons of safety or effectiveness.