78670-150 : Iwilfin 250 mg Oral Tablet


NDC: 78670-150
Labeler: Uswm, LLC
Product Type: Human Prescription Drug
Drug Name:  Iwilfin
Dosage Form: Oral Tablet
Application #: NDA215500
Rev. Date: 


NDC Package Codes:

  • 78670-150-01: 1 BOTTLE IN 1 CARTON (78670‑150‑01) / 100 TABLET IN 1 BOTTLE

Active Ingredients:

  • Eflornithine Hydrochloride

Dosage Strength:

  • 250 mg

Pharmaceutical Classes:

  • Antiprotozoal [EPC]
  • Decarboxylase Inhibitor [EPC]
  • Decarboxylase Inhibitors [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.