NDC Code | 13668-253-74 |
Package Description | 100 TABLET in 1 BOTTLE (13668-253-74) |
Product NDC | 13668-253 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Olmesartan Medoxomil And Hydrochlorothiazide |
Non-Proprietary Name | Olmesartan Medoxomil And Hydrochlorothiazide 40/25 |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20170424 |
Marketing Category Name | ANDA |
Application Number | ANDA206515 |
Manufacturer | TORRENT PHARMACEUTICALS LIMITED |
Substance Name | OLMESARTAN MEDOXOMIL; HYDROCHLOROTHIAZIDE |
Strength | 40; 25 |
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] |