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Lubiprostone

NDC 0480-4138 · HUMAN PRESCRIPTION DRUG · CAPSULE, GELATIN COATED

Labeler / ManufacturerTeva Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA209920
Dosage form / routeCAPSULE, GELATIN COATED · ORAL
Active ingredientsLUBIPROSTONE (24 ug/1)
Marketing started20230103
Package count1

External sources

Source: openFDA. Public-domain (CC0).