| NDC Code | 50228-365-30 |
|---|
| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (50228-365-30) |
|---|
| Product NDC | 50228-365 |
|---|
| 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 | 20181203 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA209010 |
|---|
| Manufacturer | ScieGen Pharmaceuticals, Inc |
|---|
| 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] |
|---|