# Sucralfate

NDC: 65162-062
Generic name: Sucralfate Oral
Labeler / Manufacturer: Amneal Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20191202

FDA application: ANDA209356

## 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:"65162-062"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65162-062
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4350b771-76a9-4e00-93f0-a18c71288f83