| NDC Code | 60505-4583-9 |
|---|
| Package Description | 90 TABLET, FILM COATED in 1 BOTTLE (60505-4583-9) |
|---|
| Product NDC | 60505-4583 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Amlodipine And Olmesartan Medoxomil |
|---|
| Non-Proprietary Name | Amlodipine And Olmesartan Medoxomil |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20170815 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA207807 |
|---|
| Manufacturer | Apotex Corp. |
|---|
| Substance Name | AMLODIPINE BESYLATE; OLMESARTAN MEDOXOMIL |
|---|
| Strength | 5; 40 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Calcium Channel Antagonists [MoA],Dihydropyridine Calcium Channel Blocker [EPC],Dihydropyridines [CS],Angiotensin 2 Receptor Antagonists [MoA],Angiotensin 2 Receptor Blocker [EPC] |
|---|