Valsartan 70771-1885
Product NDC
70771-1885- Manufacturer
- Zydus Lifesciences Limited
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 30, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA218991
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Valsartan | 320 mg/1 |
Drug Class
Angiotensin 2 Receptor Blocker [EPC]Angiotensin 2 Receptor Antagonists [MoA]Angiotensin 2 Receptor Blocker [EPC]
Packaging Options(1)
90 TABLET, FILM COATED in 1 BOTTLE (70771-1885-9)