0254-3035 : Tiopronin 300 mg Oral Tablet, Delayed Release


NDC: 0254-3035
Labeler: Endo USA, Inc.
Product Type: Human Prescription Drug
Drug Name:  Tiopronin
Dosage Form: Oral Tablet, Delayed Release
Application #: ANDA217219
Rev. Date: 


NDC Package Codes:

  • 0254-3035-09: 90 TABLET, DELAYED RELEASE IN 1 BOTTLE (0254‑3035‑09)

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.
  • 0254-3034 Tiopronin 100 mg Oral Tablet, Delayed Release by Endo USA, Inc.
  • 0093-7909 Tiopronin 100 mg Oral Tablet, Sugar Coated by Teva Pharmaceuticals USA, Inc.
  • 0480-7824 Tiopronin 300 mg Oral Tablet, Delayed Release by Teva Pharmaceuticals, Inc.
  • 0480-9227 Tiopronin 100 mg Oral Tablet, Delayed Release by Teva Pharmaceuticals, 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
  • 44523-054 Tiopronin 100 mg Oral Tablet, Delayed Release by Bio Comp Pharma, Inc.
  • 44523-055 Tiopronin 300 mg Oral Tablet, Delayed Release by Bio Comp Pharma, Inc.
  • 60219-2009 Tiopronin 300 mg Oral Tablet, Delayed Release by Amneal Pharmaceuticals Ny LLC

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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.