| NDC Code | 68210-4120-1 |
|---|
| Package Description | 1 BOTTLE in 1 CARTON (68210-4120-1) > 15 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE |
|---|
| Product NDC | 68210-4120 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Naproxen Sodium |
|---|
| Non-Proprietary Name | Naproxen Sodium |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20200323 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA207612 |
|---|
| Manufacturer | Spirit Pharmaceuticals LLC |
|---|
| Substance Name | NAPROXEN SODIUM |
|---|
| Strength | 220 |
|---|
| Strength Unit | 1/1 |
|---|
| Pharmacy Classes | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC] |
|---|