| NDC Code | 71205-063-90 |
|---|
| Package Description | 90 TABLET in 1 BOTTLE (71205-063-90) |
|---|
| Product NDC | 71205-063 |
|---|
| 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 | Proficient Rx LP |
|---|
| Substance Name | HYDROCHLOROTHIAZIDE; IRBESARTAN |
|---|
| Strength | 12.5; 150 |
|---|
| 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] |
|---|