NDC Code | 43547-393-11 |
Package Description | 1000 TABLET in 1 BOTTLE (43547-393-11) |
Product NDC | 43547-393 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Olmesartan Medoxomil And Hydrochlorothiazide |
Non-Proprietary Name | Olmesartan Medoxomil And Hydrochlorothiazide |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20170424 |
Marketing Category Name | ANDA |
Application Number | ANDA207804 |
Manufacturer | Solco Healthcare US, LLC |
Substance Name | HYDROCHLOROTHIAZIDE; OLMESARTAN MEDOXOMIL |
Strength | 25; 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] |