| NDC Code | 70000-0201-3 |
|---|
| Package Description | 1 BOTTLE in 1 CARTON (70000-0201-3) / 100 TABLET, FILM COATED in 1 BOTTLE |
|---|
| Product NDC | 70000-0201 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Leader All Day Pain Relief |
|---|
| Non-Proprietary Name | Naproxen Sodium |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20161207 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA074661 |
|---|
| Manufacturer | Cardinal Health 110, LLC. dba Leader |
|---|
| Substance Name | NAPROXEN SODIUM |
|---|
| Strength | 220 |
|---|
| Strength Unit | mg/1 |
|---|
| Pharmacy Classes | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Nonsteroidal Anti-inflammatory Drug [EPC] |
|---|