FDA NDC Directory · JSON-LD · Markdown

Sucralfate

NDC 70518-3959 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerREMEDYREPACK INC.
Marketing categoryAbbreviated NDA (generic) · App ANDA215705
Dosage form / routeTABLET · ORAL
Active ingredientsSUCRALFATE (1 g/1)
Marketing started20231213
Package count1

External sources

Source: openFDA. Public-domain (CC0).