FDA NDC Directory · JSON-LD · Markdown

Sucralfate

NDC 51655-031 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerNorthwind Health Company, LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA070848
Dosage form / routeTABLET · ORAL
Active ingredientsSUCRALFATE (1 g/1)
Marketing started20150209
Package count1

External sources

Source: openFDA. Public-domain (CC0).