NDC Code |
43063-232-30 |
Proprietary Name |
Amlodipine Besylate and Benazepril Hydrochloride |
Package Description |
30 CAPSULE in 1 BOTTLE, PLASTIC (43063-232-30) |
Product NDC |
43063-232 |
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 |
PD-Rx Pharmaceuticals, Inc. |
Substance Name |
AMLODIPINE BESYLATE; BENAZEPRIL HYDROCHLORIDE |
Strength Number |
10; 20 |
Strength Unit |
mg/1; mg/1 |
Pharmaceutical 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] |