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Labeling Requirements for Prescription Drugs and/or Insulin | Midpage
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Code of Federal Regulations
Title 21
Chapter I
Subchapter C
Part 201
Subpart B
Labeling Requirements for Prescription Drugs and/or Insulin
201.50
Statement of identity.
201.51
Declaration of net quantity of contents.
201.55
Statement of dosage.
201.56
Requirements on content and format of labeling for human prescription drug and biological products.
201.57
Specific requirements on content and format of labeling for human prescription drug and biological products described in § 201.56(b)(1).
201.58
Waiver of labeling requirements.