| NDC Code | 21695-808-30 |
|---|
| Package Description | 30 TABLET, COATED in 1 BOTTLE (21695-808-30) |
|---|
| Product NDC | 21695-808 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Bisoprolol Fumarate And Hydrochlorothiazide |
|---|
| Non-Proprietary Name | Bisoprolol Fumarate And Hydrochlorothiazide |
|---|
| Dosage Form | TABLET, COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20000925 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA075579 |
|---|
| Manufacturer | Rebel Distributors Corp |
|---|
| Substance Name | BISOPROLOL FUMARATE; HYDROCHLOROTHIAZIDE |
|---|
| Strength | 5; 6.25 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [CS] |
|---|