21 CFR 1314.05
§ 1314.05 Requirements regarding packaging of nonliquid forms.
United States · 21 CFR — Food and Drugs · Status: effective
Cite this
- Citation
- 21 CFR 1314.05, § 1314.05 Requirements regarding packaging of nonliquid forms, United States, version 1 as recorded 2026-07-09, yourstate.us, https://yourstate.us/provision/92168
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Full text
A regulated seller or mail order distributor may not sell a scheduled listed chemical product in nonliquid form (including gel caps) unless the product is packaged either in blister packs, with each blister containing no more than two dosage units or, if blister packs are technically infeasible, in unit dose packets or pouches.
Legislative history
This is a federal regulation, adopted through agency rulemaking under the Administrative Procedure Act — not enacted by a recorded vote of Congress.