NDC Code | 13668-251-30 |
Package Description | 30 TABLET in 1 BOTTLE (13668-251-30) |
Product NDC | 13668-251 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Olmesartan Medoxomil And Hydrochlorothiazide |
Non-Proprietary Name | Olmesartan Medoxomil And Hydrochlorothiazide 20/12.5 |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20170424 |
End Marketing Date | 20240531 |
Marketing Category Name | ANDA |
Application Number | ANDA206515 |
Manufacturer | Torrent Pharmaceuticals Limited |
Substance Name | HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL |
Strength | 12.5; 20 |
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] |