NDC Code | 13668-312-74 |
Package Description | 100 TABLET in 1 BOTTLE (13668-312-74) |
Product NDC | 13668-312 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Proprietary Name | Amlodipine And Olmesartan Medoxomil |
Non-Proprietary Name | Amlodipine And Olmesartan Medoxomil |
Dosage Form | TABLET |
Usage | ORAL |
Start Marketing Date | 20161125 |
Marketing Category Name | ANDA |
Application Number | ANDA202933 |
Manufacturer | Torrent Pharmaceuticals Limited |
Substance Name | AMLODIPINE; OLMESARTAN MEDOXOMIL |
Strength | 10; 20 |
Strength Unit | mg/1; mg/1 |
Pharmacy Classes | Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Calcium Channel Antagonists [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS] |