Drug application
NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE (DIPHENHYDRAMINE HYDROCHLORIDE, NAPROXEN SODIUM)
Drugs@FDA ANDA 207597 · P AND L
Key facts
| Drug name | NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE |
|---|---|
| Active ingredients | DIPHENHYDRAMINE HYDROCHLORIDE, NAPROXEN SODIUM |
| Application type | ANDA |
| Application number | 207597 |
| Company | P AND L |
| Dosage forms | TABLET, ORAL |
| Strength | 25MG;220MG |
| Marketing status | Discontinued |
| Reference listed drug | No |
| Latest submission status date | Jan 25, 2019 |
At a glance
- 1–9 Submissions
- None Label versions
- 1–9 Products
- None Therapeutic equivalents
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About Drugs@FDA applications
Drugs@FDA covers FDA-approved brand-name and generic drugs and therapeutic biologics, with their applications (NDA, ANDA or BLA), products, submissions and labels.