e-CFR data is current as of January 19, 2021 |
Title 21 → Chapter I → Subchapter C → Part 201 → Subpart A → §201.18 |
Title 21: Food and Drugs
PART 201—LABELING
Subpart A—General Labeling Provisions
The lot number on the label of a drug should be capable of yielding the complete manufacturing history of the package. An incorrect lot number may be regarded as causing the article to be misbranded.