| NDC Code | 46708-212-91 |
|---|
| Package Description | 1000 TABLET, FILM COATED in 1 BOTTLE (46708-212-91) |
|---|
| Product NDC | 46708-212 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Amlodipine Besylate And Olmesartran Medoxomil |
|---|
| Non-Proprietary Name | Amlodipine Besylate And Olmesartran Medoxomil |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20170718 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA207073 |
|---|
| Manufacturer | Alembic Pharmaceuticals Limited |
|---|
| Substance Name | AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL |
|---|
| Strength | 5; 20 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Angiotensin 2 Receptor Antagonists [MoA], Angiotensin 2 Receptor Blocker [EPC], Calcium Channel Antagonists [MoA], Calcium Channel Blocker [EPC], Cytochrome P450 3A Inhibitors [MoA], Dihydropyridine Calcium Channel Blocker [EPC], Dihydropyridines [CS] |
|---|