83114-001 : Mifepristone 200 mg Oral Tablet


NDC: 83114-001
Labeler: Pci Pharma Services Canada, Inc.
Product Type: Human Prescription Drug
Drug Name: Mifepristone
Dosage Form: Oral Tablet
Application #: ANDA091178
Rev. Date: 


NDC Package Codes:

  • 83114-001-01: 1 TABLET IN 1 BLISTER PACK (83114‑001‑01)
  • 83114-001-06: 6 TABLET IN 1 CARTON (83114‑001‑06)

Active Ingredients:

  • Mifepristone

Dosage Strength:

  • 200 mg

Pharmaceutical Classes:

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

Related Products:

Based on records with the same trade name.
  • 0591-4390 Mifepristone 300 mg Oral Tablet, Film Coated by Actavis Pharma, Inc.
  • 43393-001 Mifepristone 200 mg Oral Tablet by Genbiopro Inc
  • 76346-654 Mifepristone 300 mg Oral Tablet by Corcept Therapeutics Incorporated

NDC QR Code

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NDC 83114-001 QR Code

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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.