# KRISTALOSE

NDC: 66220-719
Generic name: lactulose
Labeler / Manufacturer: Cumberland Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER, FOR SOLUTION
Routes: ORAL
Marketing started: 20120120

FDA application: ANDA074712

## Active ingredients

- LACTULOSE: 10 g/10g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"66220-719"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=66220-719
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=535dd1ea-b567-49f7-9a84-8ea91e78c466