# Oxaprozin

NDC: 82804-261
Generic name: Oxaprozin
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20010131

FDA application: ANDA075855

## Active ingredients

- OXAPROZIN: 600 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"82804-261"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82804-261
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e3fbea8c-bc0d-4dcd-a14e-a4575dceeea6