Bisoprolol Fumarate 70771-1726
Product NDC
70771-1726- Manufacturer
- Zydus Lifesciences Limited
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- September 15, 2022
- Listing Expires
- December 31, 2026
- Application
- ANDA215680
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Bisoprolol Fumarate | 5 mg/1 |
Drug Class
Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]
Packaging Options(2)
100 TABLET, FILM COATED in 1 BOTTLE (70771-1726-1)
30 TABLET, FILM COATED in 1 BOTTLE (70771-1726-3)