FDA NDC Directory · JSON-LD · Markdown

Pomalidomide

NDC 60505-4500 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerApotex Corp.
Marketing categoryAbbreviated NDA (generic) · App ANDA210164
Dosage form / routeCAPSULE · ORAL
Active ingredientsPOMALIDOMIDE (4 mg/1)
Marketing started20260311
Package count1

External sources

Source: openFDA. Public-domain (CC0).