FDA NDC Directory · JSON-LD · Markdown

Sucralfate

NDC 82804-063 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerProficient Rx LP
Marketing categoryAbbreviated NDA (generic) · App ANDA070848
Dosage form / routeTABLET · ORAL
Active ingredientsSUCRALFATE (1 g/1)
Marketing started19961111
Package count3

External sources

Source: openFDA. Public-domain (CC0).