NDC Code | 61919-852-90 |
Package Description | 90 CAPSULE in 1 BOTTLE (61919-852-90) |
Product NDC | 61919-852 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Amoldipine Benazepril Hcl |
Non-Proprietary Name | Amoldipine Benazepril Hcl |
Dosage Form | CAPSULE |
Usage | ORAL |
Start Marketing Date | 20190422 |
Marketing Category Name | ANDA |
Application Number | ANDA202239 |
Manufacturer | DirectRX |
Substance Name | AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE |
Strength | 10; 20 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Calcium Channel Antagonists [MoA], Decreased Blood Pressure [PE], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS] |