FDA NDC Directory · JSON-LD · Markdown

Sugammadex

NDC 0264-8200 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerB. Braun Medical Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA214279
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsSUGAMMADEX SODIUM (200 mg/2mL)
Marketing started20260728
Package count1

External sources

Source: openFDA. Public-domain (CC0).