FDA NDC Directory · JSON-LD · Markdown

Lactulose

NDC 73352-900 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SOLUTION

Labeler / ManufacturerTrifluent Pharma, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA217914
Dosage form / routePOWDER, FOR SOLUTION · ORAL
Active ingredientsLACTULOSE (10 g/10g)
Marketing started20250913
Package count1

External sources

Source: openFDA. Public-domain (CC0).