Bisoprolol Fumarate And Hydrochlorothiazide 71335-1769
Product NDC
71335-1769- Manufacturer
- Bryant Ranch Prepack
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 30, 2019
- Listing Expires
- December 31, 2027
- Application
- ANDA212678
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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(4)
30 TABLET, FILM COATED in 1 BOTTLE (71335-1769-1)
90 TABLET, FILM COATED in 1 BOTTLE (71335-1769-2)
28 TABLET, FILM COATED in 1 BOTTLE (71335-1769-3)
100 TABLET, FILM COATED in 1 BOTTLE (71335-1769-4)