CFR section
21 CFR 226.80(b)(2): Packaging and labeling
PART 226-CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES · Subpart D-Packaging and Labeling
Key facts
| Citation | 21 CFR 226.80(b)(2) |
|---|---|
| Section | Packaging and labeling |
| Part | PART 226-CURRENT GOOD MANUFACTURING PRACTICE FOR TYPE A MEDICATED ARTICLES |
| Subpart | Subpart D-Packaging and Labeling |
| Subchapter | 21 CFR C Drugs General |
| Product types cited | Drugs |
| Regulation text (excerpt) | (2) For careful checking of labeling for identity and conformity to the labeling specified in the batch-production records. |
At a glance
- 1–9 Inspections citing this section
- None Warning letters citing this section
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About CFR sections cited by the FDA
Title 21 of the Code of Federal Regulations contains the FDA's regulations, including current good manufacturing practice and quality system requirements that inspections cite.