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U.S. Code of Federal Regulations
Regulations most recently checked for updates: Feb 09, 2023
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Title 21
Chapter I
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.
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