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: |
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