Bisoprolol Fumarate And Hydrochlorothiazide 68462-0878
Product NDC
68462-0878- Manufacturer
- Glenmark Pharmaceuticals Inc., Usa
- Dosage Form
- Tablet, Film Coated
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 26, 2022
- Listing Expires
- December 31, 2027
- Application
- ANDA215995
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Bisoprolol Fumarate | 2.5 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 (68462-878-01)
500 TABLET, FILM COATED in 1 BOTTLE (68462-878-05)
30 TABLET, FILM COATED in 1 BOTTLE (68462-878-30)