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Lubiprostone

NDC 72603-288 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic namelubiprostone
Labeler / ManufacturerNorthstar Rx LLC
Marketing categoryAbbreviated NDA (generic) · App ANDA218640
Dosage form / routeCAPSULE · ORAL
Active ingredientsLUBIPROSTONE (.008 mg/1)
Marketing started20250701
Package count1

External sources

Source: openFDA. Public-domain (CC0).