FDA NDC Directory · JSON-LD · Markdown
NDC 72288-310 · HUMAN OTC DRUG · TABLET, FILM COATED
| Generic name | diphenhydramine hydrochloride, naproxen sodium |
|---|---|
| Labeler / Manufacturer | Amazon.com Services LLC |
| Marketing category | Abbreviated NDA (generic) · App ANDA208499 |
| Dosage form / route | TABLET, FILM COATED · ORAL |
| Active ingredients | DIPHENHYDRAMINE HYDROCHLORIDE (25 mg/1) NAPROXEN SODIUM (220 mg/1) |
| Marketing started | 20210810 |
| Package count | 1 |
Source: openFDA. Public-domain (CC0).