# LACTULOSE Crystalline

NDC: 85592-829
Generic name: lactulose
Labeler / Manufacturer: Cumberland Assured Products Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SOLUTION
Routes: ORAL
Marketing started: 20250901

FDA application: ANDA074712

## 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:"85592-829"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=85592-829
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=59e75426-42ae-4904-941f-009181101a8a