Bisoprolol Fumarate And Hydrochlorothiazide 70771-1761
Product NDC
70771-1761- Manufacturer
- Zydus Lifesciences Limited
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 1, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA215666
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Bisoprolol Fumarate | 5 mg/1 |
| Hydrochlorothiazide | 6.25 mg/1 |
Drug Class
Thiazide Diuretic [EPC]Adrenergic beta-Antagonists [MoA]Increased Diuresis [PE]
Packaging Options(3)
100 TABLET, FILM COATED in 1 BOTTLE (70771-1761-1)
30 TABLET, FILM COATED in 1 BOTTLE (70771-1761-3)
500 TABLET, FILM COATED in 1 BOTTLE (70771-1761-5)