FDA NDC Directory · JSON-LD · Markdown

YUSIMRY

NDC 71288-817 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic nameadalimumab-aqvh
Labeler / ManufacturerMeitheal Pharmaceuticals Inc.
Marketing categoryBiologic License Application · App BLA761216
Dosage form / routeINJECTION, SOLUTION · SUBCUTANEOUS
Active ingredientsADALIMUMAB (40 mg/.4mL)
Marketing started20260925
Package count1

External sources

Source: openFDA. Public-domain (CC0).