59572-705 : Idhifa 50 mg Oral Tablet, Film Coated


NDC59572-705
Labeler: Celgene Corporation
Product Type: Human Prescription Drug
Drug Name:  Idhifa
Dosage Form: Oral Tablet, Film Coated
Application #: NDA209606
Rev. Date: 


Appearance:


Markings: ENA;50
Shapes:  Oval
Colors:  Yellow
Size (mm): 12
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:

  • 59572-705-30: 30 TABLET, FILM COATED IN 1 BOTTLE (59572‑705‑30)

Active Ingredients:

  • Enasidenib Mesylate

Dosage Strength:

  • 50 mg

Inactive Ingredients:

  • Microcrystalline Cellulose
  • Hydroxypropyl Cellulose, Unspecified
  • Sodium Starch Glycolate Type a Potato
  • Sodium Lauryl Sulfate
  • Hypromellose Acetate Succinate 06081224 (3 Mm2/S)
  • Silicon Dioxide
  • Magnesium Stearate
  • Polyvinyl Alcohol
  • Titanium Dioxide
  • Polyethylene Glycol
  • Talc
  • Ferric Oxide Yellow

Pharmaceutical Classes:

  • Isocitrate Dehydrogenase 2 Inhibitor [EPC]
  • Isocitrate Dehydrogenase 2 Inhibitors [MoA]

Related Products:

Based on records with the same trade name.
  • 59572-710 Idhifa 100 mg Oral Tablet, Film Coated by Celgene Corporation

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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.