| NDC Code: |
51079-698 |
| Proprietary Name: |
Lisinopril and Hydrochlorothiazide |
| Suffix: |
|
| Non-Proprietary Name: |
lisinopril and hydrochlorothiazide |
| Dosage Form: |
TABLET |
| Method: |
ORAL |
| Original Marketing Date: |
08-06-2010 |
| Category Name: |
ANDA |
| Application Number: |
ANDA076113 |
| Labeler: |
UDL LABORATORIES, INC. |
| Substance Name: |
HYDROCHLOROTHIAZIDE; LISINOPRIL |
| Active Numerator Strength: |
12.5; 20 |
| Active Ingredient Unit: |
mg/1; mg/1 |
| Pharm Classes: |
Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
| DEA Schedule: |
|
