| NDC Code | 76420-889-90 |
|---|
| Package Description | 90 TABLET, DELAYED RELEASE in 1 BOTTLE (76420-889-90) |
|---|
| Product NDC | 76420-889 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Naproxen And Esomeprazole Magnesium |
|---|
| Non-Proprietary Name | Naproxen And Esomeprazole Magnesium |
|---|
| Dosage Form | TABLET, DELAYED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20200218 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA204206 |
|---|
| Manufacturer | Asclemed USA, Inc. |
|---|
| Substance Name | ESOMEPRAZOLE MAGNESIUM; NAPROXEN |
|---|
| Strength | 20; 500 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Cytochrome P450 2C19 Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC], Proton Pump Inhibitor [EPC], Proton Pump Inhibitors [MoA] |
|---|