| NDC Code | 41250-526-60 |
|---|
| Package Description | 1 BOTTLE in 1 CARTON (41250-526-60) / 20 TABLET, FILM COATED in 1 BOTTLE |
|---|
| Product NDC | 41250-526 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Naproxen Sodium Pm |
|---|
| Non-Proprietary Name | Diphenhydramine Hydrochloride, Naproxen Sodium |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20200114 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA208499 |
|---|
| Manufacturer | Meijer Distribution Inc |
|---|
| Substance Name | DIPHENHYDRAMINE HYDROCHLORIDE; NAPROXEN SODIUM |
|---|
| Strength | 25; 220 |
|---|
| Strength Unit | mg/1; mg/1 |
|---|
| Pharmacy Classes | Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Nonsteroidal Anti-inflammatory Drug [EPC] |
|---|