| NDC Code |
43489-100-03 |
| Proprietary Name |
Amlodipine Besylate |
| Package Description |
500 TABLET in 1 BOTTLE, PLASTIC (43489-100-03) |
| Product NDC |
43489-100 |
| Product Type Name |
HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name |
Amlodipine Besylate |
| Dosage Form Name |
TABLET |
| Route Name |
ORAL |
| Start Marketing Date |
20110415 |
| Marketing Category Name |
ANDA |
| Labeler Name |
Secan Pharmaceuticals Inc |
| Substance Name |
AMLODIPINE BESYLATE |
| Strength Number |
5 |
| Strength Unit |
mg/1 |
| Pharmaceutical Classes |
Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [Chemical/Ingredient] |