FDA NDC Directory · JSON-LD · Markdown

LACTULOSE

NDC 0121-1154 · HUMAN PRESCRIPTION DRUG · SOLUTION

Labeler / ManufacturerPAI Holdings, LLC dba PAI Pharma
Marketing categoryAbbreviated NDA (generic) · App ANDA074623
Dosage form / routeSOLUTION · ORAL
Active ingredientsLACTULOSE (20 g/30mL)
Marketing started19660730
Package count2

External sources

Source: openFDA. Public-domain (CC0).