| Product ID | 61919-852_871e47cb-a829-9ba7-e053-2991aa0a96ea |
| NDC | 61919-852 |
| Product Type | Human Prescription Drug |
| Proprietary Name | AMOLDIPINE BENAZEPRIL HCL |
| Generic Name | Amoldipine Benazepril Hcl |
| Dosage Form | Capsule |
| Route of Administration | ORAL |
| Marketing Start Date | 2019-04-22 |
| Marketing Category | ANDA / ANDA |
| Application Number | ANDA202239 |
| Labeler Name | DirectRX |
| Substance Name | AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE |
| Active Ingredient Strength | 10 mg/1; mg/1 |
| Pharm 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] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |