| NDC Code | 0186-1095-05 |
|---|
| Package Description | 100 TABLET, FILM COATED in 1 BOTTLE (0186-1095-05) |
|---|
| Product NDC | 0186-1095 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Dutoprol |
|---|
| Non-Proprietary Name | Metoprolol Succinate And Hydrochlorothiazide |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20110916 |
|---|
| Marketing Category Name | NDA |
|---|
| Application Number | NDA021956 |
|---|
| Manufacturer | AstraZeneca LP |
|---|
| Substance Name | METOPROLOL SUCCINATE; HYDROCHLOROTHIAZIDE |
|---|
| Strength | 50; 12.5 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Adrenergic beta-Antagonists [MoA],beta-Adrenergic Blocker [EPC],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
|---|