70771-1604 : Solifenacin 5 mg Oral Tablet, Film Coated


NDC: 70771-1604
Labeler: Cadila Healthcare Limited
Product Type: Human Prescription Drug
Drug Name:  Solifenacin
Dosage Form: Oral Tablet, Film Coated
Application #: ANDA207721
Rev. Date: 


NDC Package Codes:

  • 70771-1604-3: 30 TABLET, FILM COATED IN 1 BOTTLE (70771‑1604‑3)
  • 70771-1604-9: 90 TABLET, FILM COATED IN 1 BOTTLE (70771‑1604‑9)

Active Ingredients:

  • Solifenacin Succinate

Dosage Strength:

  • 5 mg

Pharmaceutical Classes:

  • Cholinergic Muscarinic Antagonist [EPC]
  • Cholinergic Muscarinic Antagonists [MoA]

Related Products:

Based on records with the same trade name.
  • 70771-1605 Solifenacin 10 mg Oral Tablet, Film Coated by Cadila Healthcare Limited
  • 68382-987 Solifenacin 5 mg Oral Tablet, Film Coated by Zydus Pharmaceuticals USA Inc.
  • 68382-988 Solifenacin 10 mg Oral Tablet, Film Coated by Zydus Pharmaceuticals USA Inc.

NDC QR Code

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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.