21 CFR § 226.110

21 CFR · Food and Drugs

§ 226.110 — Distribution records.

21 CFR § 226.110

TitleTitle 21: Food and Drugs PartPart 226: Current Good Manufacturing Practice for Type a Medicated Articles

SourceeCFR (current through Apr 9, 2026)

This text of 21 C.F.R. § 226.110 (Distribution records.) is published on Counsel Stack Legal Research, covering United States primary law. Counsel Stack provides free access to over 12 million legal documents including statutes, case law, regulations, and constitutions.

Bluebook

21 C.F.R. § 226.110 (2026).

Text

§ 226.110 Distribution records.
Complete records shall be maintained for each shipment of Type A medicated article(s) in a manner that will facilitate the recall, diversion, or destruction of the Type A medicated article(s), if necessary. Such records shall be retained for at least 2 years after the date of the shipment by the manufacturer and shall include the name and address of the consignee, the date and quantity shipped, and the manufacturing dates, control numbers, or marks identifying the Type A medicated article(s) shipped.

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§ 226.110 Distribution records.

Complete records shall be maintained for each shipment of Type A medicated article(s) in a manner that will facilitate the recall, diversion, or destruction of the Type A medicated article(s), if necessary. Such records shall be retained for at least 2 years after the date of the shipment by the manufacturer and shall include the name and address of the consignee, the date and quantity shipped, and the manufacturing dates, control numbers, or marks identifying the Type A medicated article(s) shipped.