# Lactulose

NDC: 0121-1930
Generic name: Lactulose
Labeler / Manufacturer: PAI Holdings, LLC dba PAI Pharma
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SOLUTION
Routes: ORAL
Marketing started: 20250317

FDA application: ANDA217914

## Active ingredients

- LACTULOSE: 20 g/20g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0121-1930"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0121-1930
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5ae4b6da-44df-419a-9f2b-8c4d79f635c8