NDC Code | 68462-879-30 |
Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (68462-879-30) |
Product NDC | 68462-879 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Bisoprolol Fumarate And Hydrochlorothiazide |
Non-Proprietary Name | Bisoprolol Fumarate And Hydrochlorothiazide |
Dosage Form | TABLET, FILM COATED |
Usage | ORAL |
Start Marketing Date | 20220126 |
Marketing Category Name | ANDA |
Application Number | ANDA215995 |
Manufacturer | GLENMARK PHARMACEUTICALS INC., USA |
Substance Name | BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE |
Strength | 5; 6.25 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Adrenergic beta-Antagonists [MoA], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS], beta-Adrenergic Blocker [EPC] |