0378-2895 : Ferric Citrate 210 mg Oral Tablet, Film Coated


NDC: 0378-2895
Labeler: Mylan Pharmaceuticals Inc.
Product Type: Human Prescription Drug
Drug Name: Ferric Citrate
Dosage Form: Oral Tablet, Film Coated
Application #: NDA205874
Rev. Date: 


NDC Package Codes:

  • 0378-2895-20: 200 TABLET, FILM COATED IN 1 BOTTLE (0378‑2895‑20)

Active Ingredients:

  • Tetraferric Tricitrate Decahydrate

Dosage Strength:

  • 210 mg

Pharmaceutical Classes:

  • Iron [CS]
  • Parenteral Iron Replacement [EPC]
  • Phosphate Binder [EPC]
  • Phosphate Chelating Activity [MoA]

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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.