| NDC Code | 0480-0953-56 |
|---|
| Package Description | 30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0480-0953-56) |
|---|
| Product NDC | 0480-0953 |
|---|
| 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 | 20221101 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA075416 |
|---|
| Manufacturer | Teva Pharmaceuticals, Inc. |
|---|
| Substance Name | NAPROXEN SODIUM |
|---|
| Strength | 750 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC] |
|---|