70710-1471 : Ivabradine 5 mg Oral Tablet


NDC: 70710-1471
Labeler: Zydus Pharmaceuticals USA Inc.
Product Type: Human Prescription Drug
Drug Name:  Ivabradine
Dosage Form: Oral Tablet
Application #: ANDA213442
Rev. Date: 


NDC Package Codes:

  • 70710-1471-6: 60 TABLET IN 1 BOTTLE (70710‑1471‑6)
  • 70710-1471-8: 180 TABLET IN 1 BOTTLE (70710‑1471‑8)

Active Ingredients:

  • Ivabradine Hydrochloride

Dosage Strength:

  • 5 mg

Pharmaceutical Classes:

  • Hyperpolarization-activated Cyclic Nucleotide-gated Channel Antagonists [MoA]
  • Hyperpolarization-activated Cyclic Nucleotide-gated Channel Blocker [EPC]

Related Products:

Based on records with the same trade name.
  • 70710-1472 Ivabradine 7.5 mg Oral Tablet by Zydus Pharmaceuticals USA Inc.
  • 31722-053 Ivabradine 5 mg Oral Tablet, Film Coated by Camber Pharmaceuticals, Inc.
  • 31722-054 Ivabradine 7.5 mg Oral Tablet, Film Coated by Camber Pharmaceuticals, Inc.
  • 50742-362 Ivabradine 5 mg Oral Tablet, Film Coated by Ingenus Pharmaceuticals, LLC
  • 50742-363 Ivabradine 7.5 mg Oral Tablet, Film Coated by Ingenus Pharmaceuticals, LLC
  • 70771-1863 Ivabradine 5 mg Oral Tablet by Zydus Lifesciences Limited
  • 70771-1864 Ivabradine 7.5 mg Oral Tablet by Zydus Lifesciences 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.