FDA NDC Directory · JSON-LD · Markdown

Sucralfate

NDC 54738-005 · HUMAN PRESCRIPTION DRUG · SUSPENSION

Labeler / ManufacturerRichmond Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA216726
Dosage form / routeSUSPENSION · ORAL
Active ingredientsSUCRALFATE (1 g/10mL)
Marketing started20241121
Package count1

External sources

Source: openFDA. Public-domain (CC0).