FDA NDC Directory · JSON-LD · Markdown

Lubiprostone

NDC 60687-816 · HUMAN PRESCRIPTION DRUG · CAPSULE, GELATIN COATED

Labeler / ManufacturerAmerican Health Packaging
Marketing categoryAbbreviated NDA (generic) · App ANDA209920
Dosage form / routeCAPSULE, GELATIN COATED · ORAL
Active ingredientsLUBIPROSTONE (8 ug/1)
Marketing started20260318
Package count1

External sources

Source: openFDA. Public-domain (CC0).