| NDC Code | 51079-699-40 |
|---|
| Package Description | 100 TABLET in 1 BOTTLE, PLASTIC (51079-699-40) |
|---|
| Product NDC | 51079-699 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Lisinopril And Hydrochlorothiazide |
|---|
| Non-Proprietary Name | Lisinopril And Hydrochlorothiazide |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20100607 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA076113 |
|---|
| Manufacturer | UDL Laboratories, Inc. |
|---|
| Substance Name | HYDROCHLOROTHIAZIDE; LISINOPRIL |
|---|
| Strength | 25; 20 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
|---|