| NDC Code | 68071-2131-3 |
|---|
| Package Description | 30 TABLET in 1 BOTTLE (68071-2131-3) |
|---|
| Product NDC | 68071-2131 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Bisoprolol Fumarate And Hydrochlorothiazide |
|---|
| Non-Proprietary Name | Bisoprolol Fumarate And Hydrochlorothiazide |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20101012 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA079106 |
|---|
| Manufacturer | NuCare Pharmaceuticals, Inc. |
|---|
| Substance Name | HYDROCHLOROTHIAZIDE; BISOPROLOL FUMARATE |
|---|
| Strength | 6.25; 10 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS],Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC] |
|---|