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Regulations last checked for updates: May 14, 2025
Title 21 - Food and Drugs last revised: May 12, 2025
All Titles
Title 21
Chapter I
Part 201
Subpart B - 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.
authority:
21 U.S.C. 321
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42 U.S.C. 216
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241
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source:
40 FR 13998, Mar. 27, 1975, unless otherwise noted.
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