NDC Code | 43547-331-50 |
Package Description | 500 TABLET in 1 BOTTLE (43547-331-50) |
Product NDC | 43547-331 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Irbesartan And Hydrochlorothiazide |
Non-Proprietary Name | Irbesartan And Hydrochlorothiazide |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20140301 |
Marketing Category Name | ANDA |
Application Number | ANDA203072 |
Manufacturer | Solco Healthcare US, LLC |
Substance Name | HYDROCHLOROTHIAZIDE; IRBESARTAN |
Strength | 12.5; 300 |
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] |