NDC Code |
0093-7371-10 |
Proprietary Name |
Amlodipine Besylate and Benazepril Hydrochloride |
Package Description |
1000 CAPSULE in 1 BOTTLE (0093-7371-10) |
Product NDC |
0093-7371 |
Product Type Name |
HUMAN PRESCRIPTION DRUG |
Non Proprietary Name |
Amlodipine Besylate and Benazepril Hydrochloride |
Dosage Form Name |
CAPSULE |
Route Name |
ORAL |
Start Marketing Date |
20070521 |
Marketing Category Name |
ANDA |
Labeler Name |
Teva Pharmaceuticals USA Inc |
Substance Name |
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE |
Strength Number |
5; 10 |
Strength Unit |
mg/1; mg/1 |
Pharmaceutical 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] |