| NDC Code | 58118-2279-8 |
|---|
| Package Description | 30 CAPSULE in 1 BLISTER PACK (58118-2279-8) |
|---|
| Product NDC | 58118-2279 |
|---|
| 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 | 19950303 |
|---|
| Marketing Category Name | NDA AUTHORIZED GENERIC |
|---|
| Application Number | NDA020364 |
|---|
| Manufacturer | Clinical Solutions Wholesale |
|---|
| 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 [Chemical/Ingredient],Angiotensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE] |
|---|