| NDC Code | 69842-328-02 |
|---|
| Package Description | 20 TABLET, FILM COATED in 1 BOTTLE (69842-328-02) |
|---|
| Product NDC | 69842-328 |
|---|
| Product Type Name | HUMAN OTC DRUG |
|---|
| Proprietary Name | Naproxen Sodium Diphenhydramine Hcl |
|---|
| Non-Proprietary Name | Naproxen Sodium Diphenhydramine Hcl |
|---|
| Dosage Form | TABLET, FILM COATED |
|---|
| Usage | ORAL |
|---|
| Start Marketing Date | 20210514 |
|---|
| Marketing Category Name | ANDA |
|---|
| Application Number | ANDA213663 |
|---|
| Manufacturer | CVS PHARMACY, 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] |
|---|