70710-1556 : Selexipag 1200 ug/1 Oral Tablet, Film Coated


NDC: 70710-1556
Labeler: Zydus Pharmaceuticals (Usa) Inc.
Product Type: Human Prescription Drug
Drug Name:  Selexipag
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA214302
Rev. Date: 


NDC Package Codes:

  • 70710-1556-6: 60 TABLET, FILM COATED IN 1 BOTTLE (70710‑1556‑6)

Active Ingredients:

  • Selexipag

Dosage Strength:

  • 1200 ug/1

Pharmaceutical Classes:

  • Prostacyclin Receptor Agonist [EPC]
  • Prostacyclin Receptor Agonists [MoA]

Related Products:

Based on records with the same trade name.
  • 70710-1551 Selexipag 200 ug/1 Oral Tablet, Film Coated by Zydus Pharmaceuticals (Usa) Inc.
  • 70710-1552 Selexipag 400 ug/1 Oral Tablet, Film Coated by Zydus Pharmaceuticals (Usa) Inc.
  • 70710-1553 Selexipag 600 ug/1 Oral Tablet, Film Coated by Zydus Pharmaceuticals (Usa) Inc.
  • 70710-1554 Selexipag 800 ug/1 Oral Tablet, Film Coated by Zydus Pharmaceuticals (Usa) Inc.
  • 70710-1555 Selexipag 1000 ug/1 Oral Tablet, Film Coated by Zydus Pharmaceuticals (Usa) Inc.
  • 70710-1557 Selexipag 1400 ug/1 Oral Tablet, Film Coated by Zydus Pharmaceuticals (Usa) Inc.
  • 70710-1558 Selexipag 1600 ug/1 Oral Tablet, Film Coated by Zydus Pharmaceuticals (Usa) Inc.

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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.