21 CFR 226.80 - Packaging and labeling.
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(1) To assure that only those Type A medicated article(s) that have met the specifications established in the master-formula records shall be distributed.
(4) To identify Type A medicated article(s) with lot or control numbers that permit determination of the history of the manufacture and control of the batch of Type A medicated article(s).
(2) For careful checking of labeling for identity and conformity to the labeling specified in the batch-production records.
(3) For adequate control of the quantities of labeling issued for use with the Type A medicated article(s).
Title 21 published on 2014-04-01.
No entries appear in the Federal Register after this date, for 21 CFR Part 226.