# SULINDAC

NDC: 72789-373
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: 20090904

FDA application: ANDA072050

## Active ingredients

- SULINDAC: 150 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72789-373"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72789-373
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=eb7acb87-6565-4524-a91a-02064ea8bd1a