NDC Code |
0615-1397-39 |
Proprietary Name |
amlodipine besylate and benazepril hydrochloride |
Package Description |
30 CAPSULE in 1 BLISTER PACK (0615-1397-39) |
Product NDC |
0615-1397 |
Product Type Name |
HUMAN PRESCRIPTION DRUG |
Non Proprietary Name |
amlodipine besylate and benazepril hydrochloride |
Dosage Form Name |
CAPSULE |
Route Name |
ORAL |
Start Marketing Date |
19950303 |
Marketing Category Name |
NDA |
Labeler Name |
NCS HealthCare of KY, Inc dba Vangard Labs |
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] |