FDA NDC Directory · JSON-LD · Markdown

LACTULOSE

NDC 17856-0874 · HUMAN PRESCRIPTION DRUG · SOLUTION

Generic nameLactulose
Labeler / ManufacturerAtlantic Biologicals Corp.
Marketing categoryAbbreviated NDA (generic) · App ANDA074623
Dosage form / routeSOLUTION · ORAL
Active ingredientsLACTULOSE (10 g/15mL)
Marketing started20191203
Package count1

External sources

Source: openFDA. Public-domain (CC0).