Active substances
Diphenhydramine + Naproxen
- US FDA 6
- Health Canada 1
US FDA United States — FDA approvals (Drugs@FDA)
| Product | Strength | Form · route | Applicant | Status | First approved |
|---|---|---|---|---|---|
| ALEVE PM | 25MG;220MG | tablet · oral | BAYER HLTHCARE | Over-the-counter | 17 Jan 2014 |
| NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE | 25MG;220MG | tablet · oral | PERRIGO R AND D | Over-the-counter | 10 May 2019 |
| NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE | 25MG;220MG | tablet · oral | COREPHARMA | Over-the-counter | 22 Aug 2019 |
| NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE | 25MG;220MG | tablet · oral | GRANULES | Over-the-counter | 24 Sep 2020 |
| NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE | 25MG;220MG | tablet · oral | AMNEAL PHARMS CO | Discontinued | 23 Oct 2018 |
| NAPROXEN SODIUM AND DIPHENHYDRAMINE HYDROCHLORIDE | 25MG;220MG | tablet · oral | P AND L | Discontinued | 25 Jan 2019 |
Canada Canada — marketed products (Health Canada)
| Brand | DIN | Strength | Form · route | Company |
|---|---|---|---|---|
| ALEVE NIGHTTIME | 02444593 | 25 MG; 220 MG | TABLET · ORAL | BAYER INC |
Components
Values as published by each source: SFDA human drug list (4-2026, as published by the Council of Health Insurance; indications from the CHI Daman Drug Formulary), Drugs@FDA, EMA medicines data, Health Canada Drug Product Database (Open Government Licence – Canada), CMS NADAC, NHS Drug Tariff Part VIIIA (NHSBSA Copyright, Open Government Licence v3.0), WHO Model List of Essential Medicines (CC BY 3.0 IGO; regrouped by active substance, not created by WHO), EMA PRAC, US FDA safety-related labeling changes and MHRA Drug Safety Update (Open Government Licence v3.0). Sources and reuse. Not a substitute for the official registers or the product information.