# SULINDAC

NDC: 53489-479
Generic name: sulindac
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20090904

FDA application: ANDA072051

## Active ingredients

- SULINDAC: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"53489-479"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=53489-479
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a47e4259-d44b-4b7b-b517-841cb6840982