Bisoprolol Fumarate And Hydrochlorothiazide 00093-3242
Product NDC
00093-3242- Manufacturer
- Teva Pharmaceuticals Usa, Inc.
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 7, 2019
- Listing Expires
- December 31, 2026
- Application
- NDA020186
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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(1)
100 TABLET, FILM COATED in 1 BOTTLE (0093-3242-01)