# SULINDAC

NDC: 42806-018
Generic name: SULINDAC
Labeler / Manufacturer: Epic Pharma, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20100125

FDA application: ANDA072710

## 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:"42806-018"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42806-018
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=96c73bd2-4577-487d-a642-bd8f91e94c3a