0591-4390 : Mifepristone 300 mg Oral Tablet, Film Coated


NDC: 0591-4390
Labeler: Actavis Pharma, Inc.
Product Type: Human Prescription Drug
Drug Name: Mifepristone
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA211436
Rev. Date: 


NDC Package Codes:

  • 0591-4390-96: 28 TABLET, FILM COATED IN 1 BOTTLE (0591‑4390‑96)

Active Ingredients:

  • Mifepristone

Dosage Strength:

  • 300 mg

Pharmaceutical Classes:

  • Progestational Hormone Receptor Antagonists [MoA]
  • Progestin Antagonist [EPC]

Related Products:

Based on records with the same trade name.
  • 43393-001 Mifepristone 200 mg Oral Tablet by Genbiopro Inc
  • 83114-001 Mifepristone 200 mg Oral Tablet by Pci Pharma Services Canada, Inc.

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Note: The RxChat NDC Database uses publicly available data from the FDA and the U.S. National Library of Medicine (NLM); The NLM is not responsible for the data presented and does not endorse or recommend this or any other product. While we make every effort to ensure that the information presented is accurate, you should assume that all results are unvalidated. To report any errors or inconsistencies please contact us.