# Sucralfate

NDC: 54738-005
Generic name: Sucralfate
Labeler / Manufacturer: Richmond Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SUSPENSION
Routes: ORAL
Marketing started: 20241121

FDA application: ANDA216726

## Active ingredients

- SUCRALFATE: 1 g/10mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"54738-005"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=54738-005
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7ac10c3f-9d50-4702-900c-41075ac6f896