# OXAPROZIN

NDC: 62135-176
Generic name: OXAPROZIN
Labeler / Manufacturer: Chartwell RX, LLC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20040902

FDA application: ANDA075987

## 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:"62135-176"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62135-176
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=db349233-9f09-471c-aeee-f91338d2ffe9