| NDC Code | 70756-315-99 |
|---|
| Package Description | 10 BLISTER PACK in 1 CARTON (70756-315-99) / 10 TABLET in 1 BLISTER PACK |
|---|
| Product NDC | 70756-315 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Telmisartan And Hydrochlorothiazide |
|---|
| Non-Proprietary Name | Telmisartan And Hydrochlorothiazide |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20250325 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA218406 |
|---|
| Manufacturer | Lifestar Pharma LLC |
|---|
| Substance Name | HYDROCHLOROTHIAZIDE; TELMISARTAN |
|---|
| Strength | 12.5; 40 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Increased Diuresis [PE], Thiazide Diuretic [EPC], Thiazides [CS] |
|---|