| NDC Code | 59651-678-01 |
|---|
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (59651-678-01) |
|---|
| Product NDC | 59651-678 |
|---|
| 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 | 20260121 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA217922 |
|---|
| Manufacturer | Aurobindo Pharma Limited |
|---|
| Substance Name | BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE |
|---|
| Strength | 2.5; 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] |
|---|