FDA NDC Directory · JSON-LD · Markdown

Pomalidomide

NDC 0781-2358 · HUMAN PRESCRIPTION DRUG · CAPSULE

Generic namepomalidomide
Labeler / ManufacturerSandoz Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA220741
Dosage form / routeCAPSULE · ORAL
Active ingredientsPOMALIDOMIDE (2 mg/1)
Marketing started20260901
Package count1

External sources

Source: openFDA. Public-domain (CC0).