# Naproxen Sodium Headache Pain

NDC: 43598-072
Generic name: Naproxen Sodium
Labeler / Manufacturer: Dr.Reddy's Laboratories Inc
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, COATED
Routes: ORAL
Marketing started: 20211210

FDA application: ANDA075168

## 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:"43598-072"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-072
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=12e45b43-eca2-73f4-1d68-07d4238f8c70