| NDC Code: |
60505-0207 |
| Proprietary Name: |
Lisinopril and Hydrochlorothiazide |
| Suffix: |
|
| Non-Proprietary Name: |
Lisinopril and Hydrochlorothiazide |
| Dosage Form: |
TABLET |
| Method: |
ORAL |
| Original Marketing Date: |
24-07-2008 |
| Category Name: |
ANDA |
| Application Number: |
ANDA076674 |
| Labeler: |
APOTEX CORP. |
| Substance Name: |
HYDROCHLOROTHIAZIDE; LISINOPRIL |
| Active Numerator Strength: |
25; 20 |
| Active Ingredient Unit: |
mg/1; mg/1 |
| Pharm Classes: |
Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
| DEA Schedule: |
|
