NDC Code | 46708-444-30 |
Package Description | 30 TABLET in 1 BOTTLE (46708-444-30) |
Product NDC | 46708-444 |
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 | 20160523 |
Marketing Category Name | ANDA |
Application Number | ANDA091370 |
Manufacturer | Alembic Pharmaceuticals Limited |
Substance Name | HYDROCHLOROTHIAZIDE; IRBESARTAN |
Strength | 25; 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] |