FDA NDC Directory · JSON-LD · Markdown

Sucralfate

NDC 72189-429 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerDirect_Rx
Marketing categoryAbbreviated NDA (generic) · App ANDA074415
Dosage form / routeTABLET · ORAL
Active ingredientsSUCRALFATE (1 g/1)
Marketing started20230302
Package count2

External sources

Source: openFDA. Public-domain (CC0).