# sucralfate

NDC: 0378-9205
Generic name: sucralfate
Labeler / Manufacturer: Mylan Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20220922

FDA application: ANDA212913

## 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:"0378-9205"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0378-9205
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1e781cc0-24ec-4028-8262-dcef9873ea1f