| NDC Code | 42658-141-01 |
|---|
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (42658-141-01) |
|---|
| Product NDC | 42658-141 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Irbesartan And Hydrochlorothiazide |
|---|
| Non-Proprietary Name | Irbesartan And Hydrochlorothiazide |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20170101 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA207896 |
|---|
| Manufacturer | Hisun Pharmaceuticals USA Inc. |
|---|
| Substance Name | IRBESARTAN; HYDROCHLOROTHIAZIDE |
|---|
| Strength | 150; 12.5 |
|---|
| 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] |
|---|