Lactulose
- Product NDC
- 18124-001
- 11-digit product format
- 181240001
- Labeler code
- 18124
- Product ID
- 18124-001_77d2be8d-b993-4458-97e7-86a4cb3505c8
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Lactulose
- Dosage form
- SOLUTION
- Route
- ORAL
- Labeler
- Fresenius Kabi Austria GmbH
- Application
- ANDA090503
- Marketing category
- ANDA
- Marketing start
- 2012-12-10
- Marketing end
- 0000-00-00
- Substance
- LACTULOSE
- Active strength
- 10 g/15mL
- Pharmacologic classes
- Osmotic Laxative [EPC],Osmotic Activity [MoA],Acidifying Activity [MoA],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
- NDC exclude flag
- E
- Listing certified through
- 2018-12-31
- Current FDA listing
- Historical FDA.report record