FDA NDC Directory · JSON-LD · Markdown

Sucralfate

NDC 68788-8779 · HUMAN PRESCRIPTION DRUG · TABLET

Labeler / ManufacturerPreferred Pharmaceuticals Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA215705
Dosage form / routeTABLET · ORAL
Active ingredientsSUCRALFATE (1 g/1)
Marketing started20241210
Package count2

External sources

Source: openFDA. Public-domain (CC0).