# Sulfasalazine

NDC: 11534-201
Generic name: Sulfasalazine
Labeler / Manufacturer: Sunrise Pharmaceutical, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, DELAYED RELEASE
Routes: ORAL
Marketing started: 20251211

FDA application: ANDA075339

## Active ingredients

- SULFASALAZINE: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"11534-201"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=11534-201
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d596ac59-b643-4181-80ba-f2db1cc3459c