NDC Code | 62332-116-30 |
Package Description | 30 TABLET in 1 BOTTLE (62332-116-30) |
Product NDC | 62332-116 |
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 | 20151015 |
Marketing Category Name | ANDA |
Application Number | ANDA202870 |
Manufacturer | Alembic Pharmaceuticals Inc. |
Substance Name | HYDROCHLOROTHIAZIDE; METOPROLOL TARTRATE |
Strength | 25; 100 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Adrenergic beta-Antagonists [MoA], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS], beta-Adrenergic Blocker [EPC] |