| NDC Code | 33342-129-07 |
|---|
| Package Description | 30 TABLET in 1 BOTTLE (33342-129-07) |
|---|
| Product NDC | 33342-129 |
|---|
| 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 | 20151102 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA204169 |
|---|
| Manufacturer | Macleods Pharmaceuticals Limited |
|---|
| Substance Name | TELMISARTAN; HYDROCHLOROTHIAZIDE |
|---|
| Strength | 80; 12.5 |
|---|
| 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] |
|---|