NDC Code | 35356-965-90 |
Package Description | 90 CAPSULE in 1 BOTTLE (35356-965-90) |
Product NDC | 35356-965 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Amlodipine Besylate And Benazepril Hydrochloride |
Non-Proprietary Name | Amlodipine Besylate And Benazepril Hydrochloride |
Dosage Form | CAPSULE |
Usage | ORAL |
Start Marketing Date | 19950303 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Application Number | NDA020364 |
Manufacturer | Lake Erie Medical DBA Quality Care Products LLC |
Substance Name | AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE |
Strength | 5; 40 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient],Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE] |