FDA Discontinues Lactulose Oral/Rectal Solution (NDA017906)

The FDA’s database shows that the Lactulose product (brand name Lactulose) is an oral and rectal solution marketed under product number 001. It contains the active ingredient Lactulose at a strength of 10 g/15 mL and is not a reference drug. According to the FDA entry, the marketing status of this product is listed as discontinued. The application is identified by NDA017906 and the sponsor is Solvay.