# NAPROXEN SODIUM

NDC: 49483-608
Generic name: NAPROXEN SODIUM
Labeler / Manufacturer: TIME CAP LABORATORIES, INC
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20160328

FDA application: ANDA090545

## 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:"49483-608"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=49483-608
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ab7b7b8e-923b-4dc1-812c-78e85de1bee1