| NDC Code | 24979-252-01 |
|---|
| Package Description | 100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (24979-252-01) |
|---|
| Product NDC | 24979-252 |
|---|
| Product Type Name | HUMAN PRESCRIPTION DRUG |
|---|
| Proprietary Name | Naproxen Sodium |
|---|
| Non-Proprietary Name | Naproxen Sodium |
|---|
| Dosage Form | TABLET, FILM COATED, EXTENDED RELEASE |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20240425 |
|---|
| Marketing Category Name | NDA AUTHORIZED GENERIC |
|---|
| Application Number | NDA020353 |
|---|
| Manufacturer | Upsher-Smith Laboratories, LLC |
|---|
| Substance Name | NAPROXEN SODIUM |
|---|
| Strength | 375 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC] |
|---|