# Sucralfate

NDC: 48433-226
Generic name: Sucralfate
Labeler / Manufacturer: Safecor Health, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20260716

FDA application: ANDA217126

## Active ingredients

- SUCRALFATE: 1 g/10mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"48433-226"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=48433-226
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=526f6ebc-557c-4c53-8118-1907baa0820a