72065-001 : Keveyis 50 mg Oral Tablet


NDC: 72065-001
Labeler: Xeris Pharmaceuticals, Inc.
Product Type: Human Prescription Drug
Drug Name: Keveyis
Dosage Form: Oral Tablet
Application #: NDA011366
Rev. Date: 


NDC Package Codes:

  • 72065-001-01: 100 TABLET IN 1 BOTTLE (72065‑001‑01)

Active Ingredients:

  • Dichlorphenamide

Dosage Strength:

  • 50 mg

Pharmaceutical Classes:

  • Carbonic Anhydrase Inhibitor [EPC]
  • Carbonic Anhydrase Inhibitors [MoA]
  • Sulfonamides [CS]

Related Products:

Based on records with the same trade name.
  • 51672-4177 Keveyis 50 mg Oral Tablet by Taro Pharmaceuticals U.S.a., Inc.
  • 71090-001 Keveyis 50 mg Oral Tablet by Strongbridge Us Inc.

NDC QR Code

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NDC 72065-001 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.