# Rapidol Naproxen

NDC: 55758-048
Generic name: Naproxen sodium
Labeler / Manufacturer: Pharmadel LLC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20191009

FDA application: ANDA091353

## Active ingredients

- NAPROXEN SODIUM: 220 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55758-048"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55758-048
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c94c4b6e-a48b-cee5-e053-2995a90a49ac