| NDC Code: |
0781-2271 |
| Proprietary Name: |
Amlodipine Besylate and Benazepril Hydrochloride |
| Suffix: |
|
| Non-Proprietary Name: |
amlodipine besylate and benazepril hydrochloride |
| Dosage Form: |
CAPSULE |
| Method: |
ORAL |
| Original Marketing Date: |
03-03-1995 |
| Category Name: |
NDA AUTHORIZED GENERIC |
| Application Number: |
NDA020364 |
| Labeler: |
SANDOZ INC |
| Substance Name: |
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE |
| Active Numerator Strength: |
2.5; 10 |
| Active Ingredient Unit: |
mg/1; mg/1 |
| Pharm Classes: |
Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient],Angiontensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE] |
| DEA Schedule: |
|
