| NDC Code | 0093-7671-01 |
|---|
| Package Description | 100 CAPSULE in 1 BOTTLE (0093-7671-01) |
|---|
| Product NDC | 0093-7671 |
|---|
| 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 | 20110720 |
|---|
| End Marketing Date | 20200531 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA077179 |
|---|
| Manufacturer | Teva Pharmaceuticals USA, Inc. |
|---|
| Substance Name | AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE |
|---|
| Strength | 10; 40 |
|---|
| 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] |
|---|