FDA NDC Directory · JSON-LD · Markdown

LACTULOSE Crystalline

NDC 85592-829 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SOLUTION

Generic namelactulose
Labeler / ManufacturerCumberland Assured Products Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA074712
Dosage form / routePOWDER, FOR SOLUTION · ORAL
Active ingredientsLACTULOSE (20 g/20g)
Marketing started20250901
Package count1

External sources

Source: openFDA. Public-domain (CC0).