FDA NDC Directory · JSON-LD · Markdown

Lubiprostone

NDC 60687-827 · HUMAN PRESCRIPTION DRUG · CAPSULE, GELATIN COATED

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA209920
Dosage form / routeCAPSULE, GELATIN COATED · ORAL
Active ingredientsLUBIPROSTONE (24 ug/1)
Marketing started20251126
Package count1

External sources

Source: openFDA. Public-domain (CC0).