FDA NDC Directory · JSON-LD · Markdown

Pomalidomide

NDC 0781-2354 · HUMAN PRESCRIPTION DRUG · CAPSULE

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

External sources

Source: openFDA. Public-domain (CC0).