FDA NDC Directory · JSON-LD · Markdown

Amitza

NDC 72189-410 · HUMAN PRESCRIPTION DRUG · CAPSULE, GELATIN COATED

Generic nameLubiprostone
Labeler / ManufacturerDirect_Rx
Marketing categoryAbbreviated NDA (generic) · App ANDA209920
Dosage form / routeCAPSULE, GELATIN COATED · ORAL
Active ingredientsLUBIPROSTONE (8 ug/1)
Marketing started20230112
Package count1

External sources

Source: openFDA. Public-domain (CC0).