Labeling Requirements for Prescription Drugs and/or Insulin

  1. Law
  2. CFR 21
  3. Food and Drugs
  4. Food and Drug Administration, Department of Health and Human Services
  5. Drugs: General
  6. Labeling
  7. Labeling Requirements for Prescription Drugs and/or Insulin

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Section
201.50

Statement of identity.

Section
201.51

Declaration of net quantity of contents.

Section
201.55

Statement of dosage.

Section
201.56

Requirements on content and format of labeling for human prescription drug and biological products.

Section
201.57

Specific requirements on content and format of labeling for human prescription drug and biological products described in § 201.56(b)(1).

Section
201.58

Waiver of labeling requirements.