# Sucralfate

NDC: 70518-3959
Generic name: Sucralfate
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20231213

FDA application: ANDA215705

## Active ingredients

- SUCRALFATE: 1 g/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-3959"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-3959
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c0ee24dd-de9c-4d24-b8d8-c45b02752c1c