60219-2009 : Tiopronin 300 mg Oral Tablet, Delayed Release


NDC: 60219-2009
Labeler: Amneal Pharmaceuticals Ny LLC
Product Type: Human Prescription Drug
Drug Name:  Tiopronin
Dosage Form: Oral Tablet, Delayed Release
Application #: ANDA216278
Rev. Date: 


NDC Package Codes:

  • 60219-2009-9: 90 TABLET, DELAYED RELEASE IN 1 BOTTLE (60219‑2009‑9)

Active Ingredients:

  • Tiopronin

Dosage Strength:

  • 300 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.
  • 0093-7909 Tiopronin 100 mg Oral Tablet, Sugar Coated by Teva Pharmaceuticals USA, Inc.
  • 13668-691 Tiopronin 100 mg Oral Tablet, Delayed Release by Torrent Pharmaceuticals Limited
  • 13668-692 Tiopronin 300 mg Oral Tablet, Delayed Release by Torrent Pharmaceuticals Limited

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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.