21 CFR Part 205 - GUIDELINES FOR STATE LICENSING OF WHOLESALE PRESCRIPTION DRUG DISTRIBUTORS

eCFR
Authorities (U.S. Code)

§ 205.1 Scope.
§ 205.2 Purpose.
§ 205.3 Definitions.
§ 205.4 Wholesale drug distributor licensing requirement.
§ 205.5 Minimum required information for licensure.
§ 205.6 Minimum qualifications.
§ 205.7 Personnel.
§ 205.8 Violations and penalties.
§ 205.50 Minimum requirements for the storage and handling of prescription drugs and for the establishment and maintenance of prescription drug distribution records.

Authority:

Source:

55 FR 38023, Sept. 14, 1990, unless otherwise noted.

This is a list of United States Code sections, Statutes at Large, Public Laws, and Presidential Documents, which provide rulemaking authority for this CFR Part.

This list is taken from the Parallel Table of Authorities and Rules provided by GPO [Government Printing Office].

It is not guaranteed to be accurate or up-to-date, though we do refresh the database weekly. More limitations on accuracy are described at the GPO site.

United States Code

U.S. Code: Title 21 - FOOD AND DRUGS

§ 351 - Adulterated drugs and devices

§ 352 - Misbranded drugs and devices

§ 353 - Exemptions and consideration for certain drugs, devices, and biological products

§ 371 - Regulations and hearings

§ 374 - Inspection