# SULINDAC

NDC: 24658-771
Generic name: SULINDAC
Labeler / Manufacturer: PuraCap Laboratories LLC dba Blu Pharmaceuticals
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20161114

FDA application: ANDA072711

## 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:"24658-771"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=24658-771
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0feabf47-8d0d-48c0-b263-43db4969f39e