# LACTULOSE

NDC: 0121-1154
Generic name: LACTULOSE
Labeler / Manufacturer: PAI Holdings, LLC dba PAI Pharma
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 19660730

FDA application: ANDA074623

## Active ingredients

- LACTULOSE: 20 g/30mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0121-1154"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0121-1154
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0f19e4ed-c90a-4330-a7fa-bf911aa98f09