| NDC Code | 46708-115-10 |
|---|
| Package Description | 100 TABLET in 1 BOTTLE (46708-115-10) |
|---|
| Product NDC | 46708-115 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Metoprolol Tartrate And Hydrochlorothiazide |
|---|
| Non-Proprietary Name | Metoprolol Tartrate And Hydrochlorothiazide |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20130917 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA202870 |
|---|
| Manufacturer | Alembic Pharmaceuticals Limited |
|---|
| Substance Name | HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE |
|---|
| Strength | 25; 50 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Adrenergic beta-Antagonists [MoA], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS], beta-Adrenergic Blocker [EPC] |
|---|