# Sulindac

NDC: 55289-930
Generic name: Sulindac
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 19900403

FDA application: ANDA071795

## 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:"55289-930"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55289-930
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=68d4eeed-2501-494b-b979-502720de86c0