| NDC Code: |
60505-0205 |
| Proprietary Name: |
Lisinopril and Hydrochlorothiazide |
| Suffix: |
|
| Non-Proprietary Name: |
Lisinopril and Hydrochlorothiazide |
| Dosage Form: |
TABLET |
| Method: |
ORAL |
| Original Marketing Date: |
18-07-2008 |
| Category Name: |
ANDA |
| Application Number: |
ANDA076674 |
| Labeler: |
APOTEX CORP. |
| 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: |
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