NDC Code |
54868-5792-0 |
Proprietary Name |
Amlodipine Besylate and Benazepril Hydrochloride |
Package Description |
30 CAPSULE in 1 BOTTLE (54868-5792-0) |
Product NDC |
54868-5792 |
Product Type Name |
HUMAN PRESCRIPTION DRUG |
Non Proprietary Name |
Amlodipine Besylate and Benazepril Hydrochloride |
Dosage Form Name |
CAPSULE |
Route Name |
ORAL |
Start Marketing Date |
20070628 |
Marketing Category Name |
ANDA |
Labeler Name |
Physicians Total Care, Inc. |
Substance Name |
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE |
Strength Number |
5; 10 |
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] |