| NDC Code | 23155-925-05 |
|---|
| Package Description | 500 CAPSULE in 1 BOTTLE (23155-925-05) |
|---|
| Product NDC | 23155-925 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Amlodipine And Benazepril Hydrochloride |
|---|
| Non-Proprietary Name | Amlodipine And Benazepril Hydrochloride |
|---|
| Dosage Form | CAPSULE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20251015 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA091431 |
|---|
| Manufacturer | Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc. |
|---|
| Substance Name | AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE |
|---|
| Strength | 10; 40 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Angiotensin Converting Enzyme Inhibitor [EPC], Angiotensin-converting Enzyme Inhibitors [MoA], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Decreased Blood Pressure [PE], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS] |
|---|