NDC Code | 13668-161-72 |
Package Description | 30 TABLET in 1 CARTON (13668-161-72) |
Product NDC | 13668-161 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Telmisartan And Hydrochlorthiazide |
Non-Proprietary Name | Telmisartan And Hydrochlorthiazide |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20140225 |
Marketing Category Name | ANDA |
Application Number | ANDA201192 |
Manufacturer | Torrent Pharmaceuticals Limited |
Substance Name | HYDROCHLOROTHIAZIDE; TELMISARTAN |
Strength | 25; 80 |
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] |