| NDC Code |
43063-171-14 |
| Proprietary Name |
Amlodipine Besylate and Benazepril Hydrochloride |
| Package Description |
14 CAPSULE in 1 BOTTLE (43063-171-14) |
| Product NDC |
43063-171 |
| 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 |
2.5; 10 |
| 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] |