Bisoprolol Fumarate 70095-0019
Product NDC
70095-0019- Manufacturer
- Sun Pharmaceutical Industries Limited
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 10, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA217617
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Bisoprolol Fumarate | 10 mg/1 |
Drug Class
Adrenergic beta-Antagonists [MoA]beta-Adrenergic Blocker [EPC]
Packaging Options(2)
30 TABLET, FILM COATED in 1 BOTTLE, UNIT-DOSE (70095-019-01)
100 TABLET, FILM COATED in 1 BOTTLE (70095-019-02)