FDA NDC Directory · JSON-LD · Markdown

LENALIDOMIDE

NDC 70710-1035 · HUMAN PRESCRIPTION DRUG · CAPSULE

Labeler / ManufacturerZydus Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA210154
Dosage form / routeCAPSULE · ORAL
Active ingredientsLENALIDOMIDE (25 mg/1)
Marketing started20220912
Package count2

External sources

Source: openFDA. Public-domain (CC0).