| NDC Code | 62011-0396-1 |
|---|
| Package Description | 1 BOTTLE, PLASTIC in 1 BOX (62011-0396-1) / 20 TABLET in 1 BOTTLE, PLASTIC |
|---|
| Product NDC | 62011-0396 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Naproxen Sodium Pm |
|---|
| Non-Proprietary Name | Naproxen Sodium |
|---|
| Dosage Form | TABLET |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20190131 |
|---|
| End Marketing Date | 20270131 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA209726 |
|---|
| Manufacturer | Strategic Sourcing Services LLC |
|---|
| 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] |
|---|