| NDC Code: |
60505-0209 |
| Proprietary Name: |
Enalapril Maleate and Hydrochlorothiazide |
| Suffix: |
|
| Non-Proprietary Name: |
Enalapril maleate and hydrochlorothiazide |
| Dosage Form: |
TABLET |
| Method: |
ORAL |
| Original Marketing Date: |
19-06-2007 |
| Category Name: |
ANDA |
| Application Number: |
ANDA076486 |
| Labeler: |
APOTEX CORP. |
| Substance Name: |
ENALAPRIL MALEATE; HYDROCHLOROTHIAZIDE |
| Active Numerator Strength: |
10; 25 |
| Active Ingredient Unit: |
mg/1; mg/1 |
| Pharm Classes: |
Angiontensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE],Increased Diuresis [PE],Thiazide Diuretic [EPC],Thiazides [Chemical/Ingredient] |
| DEA Schedule: |
|
