70709-121 : Venxxiva 100 mg Oral Tablet, Delayed Release


NDC: 70709-121
Labeler: Cycle Pharmaceuticals Ltd.
Product Type: Human Prescription Drug
Drug Name:  Venxxiva
Dosage Form: Oral Tablet, Delayed Release
Application #: ANDA216990
Rev. Date: 


NDC Package Codes:

  • 70709-121-30: 300 TABLET, DELAYED RELEASE IN 1 BOTTLE (70709‑121‑30)

Active Ingredients:

  • Tiopronin

Dosage Strength:

  • 100 mg

Pharmaceutical Classes:

  • Cystine Disulfide Reduction [MoA]
  • N-substituted Glycines [CS]
  • Reducing and Complexing Thiol [EPC]

Related Products:

Based on records with the same trade name.
  • 70709-123 Venxxiva 300 mg Oral Tablet, Delayed Release by Cycle Pharmaceuticals Ltd.

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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.