# Lubiprostone

NDC: 72603-288
Generic name: lubiprostone
Labeler / Manufacturer: Northstar Rx LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CAPSULE
Routes: ORAL
Marketing started: 20250701

FDA application: ANDA218640

## Active ingredients

- LUBIPROSTONE: .008 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72603-288"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72603-288
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1626ac65-ea12-421b-9780-bfdb50a39e1a