FDA NDC Directory · JSON-LD · Markdown

Lenalidomide

NDC 63304-044 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerSun Pharmaceutical Industries, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA211846
Dosage form / routeCAPSULE · ORAL
Active ingredientsLENALIDOMIDE (15 mg/1)
Marketing started20230304
Package count2

External sources

Source: openFDA. Public-domain (CC0).