FDA NDC Directory · JSON-LD · Markdown

Carafate

NDC 58914-171 · HUMAN PRESCRIPTION DRUG · TABLET

Generic nameSucralfate
Labeler / ManufacturerAllergan, Inc.
Marketing categoryNew Drug Application (innovator) · App NDA018333
Dosage form / routeTABLET · ORAL
Active ingredientsSUCRALFATE (1 g/1)
Marketing started19811030
Package count1

External sources

Source: openFDA. Public-domain (CC0).