| NDC Code: |
50436-7000 |
| Proprietary Name: |
LISINOPRIL AND HYDROCHLOROTHIAZIDE |
| Suffix: |
|
| Non-Proprietary Name: |
LISINOPRIL AND HYDROCHLOROTHIAZIDE |
| Dosage Form: |
TABLET |
| Method: |
ORAL |
| Original Marketing Date: |
04-10-2006 |
| Category Name: |
ANDA |
| Application Number: |
ANDA077912 |
| Labeler: |
UNIT DOSE SERVICES |
| Substance Name: |
HYDROCHLOROTHIAZIDE; LISINOPRIL |
| Active Numerator Strength: |
12.5; 10 |
| Active Ingredient Unit: |
mg/1; mg/1 |
| Pharm Classes: |
Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient],Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA] |
| DEA Schedule: |
|
