| NDC Code: |
0185-0124 |
| Proprietary Name: |
Benazepril Hydrochloride and Hydrochlorothiazide |
| Suffix: |
|
| Non-Proprietary Name: |
Benazepril Hydrochloride and Hydrochlorothiazide |
| Dosage Form: |
TABLET, FILM COATED |
| Method: |
ORAL |
| Original Marketing Date: |
11-02-2004 |
| End of Marketing: |
30-09-2015 |
| Category Name: |
ANDA |
| Application Number: |
ANDA076631 |
| Labeler: |
EON LABS, INC. |
| Substance Name: |
BENAZEPRIL HYDROCHLORIDE; HYDROCHLOROTHIAZIDE |
| Active Numerator Strength: |
5; 6.25 |
| 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: |
|
