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KRISTALOSE

NDC 66220-719 · HUMAN PRESCRIPTION DRUG · POWDER, FOR SOLUTION

Generic namelactulose
Labeler / ManufacturerCumberland Pharmaceuticals Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA074712
Dosage form / routePOWDER, FOR SOLUTION · ORAL
Active ingredientsLACTULOSE (10 g/10g)
Marketing started20120120
Package count1

External sources

Source: openFDA. Public-domain (CC0).