FDA NDC Directory · JSON-LD · Markdown

ZALTRAP

NDC 0024-5841 · HUMAN PRESCRIPTION DRUG · SOLUTION, CONCENTRATE

Generic nameziv-aflibercept
Labeler / Manufacturersanofi-aventis U.S. LLC
Marketing categoryBiologic License Application · App BLA125418
Dosage form / routeSOLUTION, CONCENTRATE · INTRAVENOUS
Active ingredientsAFLIBERCEPT (200 mg/8mL)
Marketing started20120803
Package count1

External sources

Source: openFDA. Public-domain (CC0).