# Sucralfate

NDC: 17856-0306
Generic name: Sucralfate
Labeler / Manufacturer: ATLANTIC BIOLOGICALS CORP.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20220315

FDA application: ANDA211884

## 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:"17856-0306"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=17856-0306
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e5073597-ac51-4e7c-a9dc-7695773a01f1