43393-001 : Mifepristone 200 mg Oral Tablet


NDC: 43393-001
Labeler: Genbiopro Inc
Product Type: Human Prescription Drug
Drug Name: Mifepristone
Dosage Form: Oral Tablet
Application #: ANDA091178
Rev. Date: 


Appearance:


Markings: S
Shapes:  Round
Colors:  Yellow
Size (mm): 11
Segments: * 1

* Segments = the number of equally sized pieces which the pill can be broken into. In this case, a value of 1 indicates a solid pill with no score lines.

NDC Package Codes:

  • 43393-001-06: 6 CARTON IN 1 PACKAGE (43393‑001‑06) > 1 BLISTER PACK IN 1 CARTON > 1 TABLET IN 1 BLISTER PACK (43393‑001‑01)

Active Ingredients:

  • Mifepristone

Dosage Strength:

  • 200 mg

Inactive Ingredients:

  • Silicon Dioxide
  • Starch, Corn
  • Povidone, Unspecified
  • Microcrystalline Cellulose
  • Magnesium Stearate /

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.
  • 83114-001 Mifepristone 200 mg Oral Tablet by Pci Pharma Services Canada, Inc.

NDC QR Code

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NDC 43393-001 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.