Federal (United States) · Regulations
Subpart B
6 sections
6 sections
- 21 C.F.R. § 201.50Statement of identity.
- 21 C.F.R. § 201.51Declaration of net quantity of contents.
- 21 C.F.R. § 201.55Statement of dosage.
- 21 C.F.R. § 201.56Requirements on content and format of labeling for human prescription drug and biological products.
- 21 C.F.R. § 201.57Specific requirements on content and format of labeling for human prescription drug and biological products described in § 201.56(b)(1).
- 21 C.F.R. § 201.58Waiver of labeling requirements.