# Sucralfate

NDC: 13668-754
Generic name: Sucralfate
Labeler / Manufacturer: Torrent Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20250915

FDA application: ANDA216726

## 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:"13668-754"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=13668-754
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dc361b46-fda4-4b0b-9950-e8885ba5b084