NDC Code | 68071-1956-3 |
Package Description | 30 CAPSULE in 1 BOTTLE (68071-1956-3) |
Product NDC | 68071-1956 |
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 | 20100419 |
Marketing Category Name | ANDA |
Application Number | ANDA077183 |
Manufacturer | NuCare Pharmaceuticals, Inc. |
Substance Name | AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE |
Strength | 2.5; 10 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS],Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE] |