| NDC Code |
54868-5782-2 |
| Proprietary Name |
Amlodipine Besylate and Benazepril Hydrochloride |
| Package Description |
100 CAPSULE in 1 BOTTLE (54868-5782-2) |
| Product NDC |
54868-5782 |
| Product Type Name |
HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name |
Amlodipine Besylate and Benazepril Hydrochloride |
| Dosage Form Name |
CAPSULE |
| Route Name |
ORAL |
| Start Marketing Date |
20070626 |
| Marketing Category Name |
ANDA |
| Labeler Name |
Physicians Total Care, Inc. |
| Substance Name |
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE |
| Strength Number |
5; 20 |
| Strength Unit |
mg/1; mg/1 |
| Pharmaceutical Classes |
Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient],Angiontensin Converting Enzyme Inhibitor [EPC],Angiotensin-converting Enzyme Inhibitors [MoA],Decreased Blood Pressure [PE] |