FDA NDC Directory · JSON-LD · Markdown

Sugammadex

NDC 0781-3468 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Generic namesugammadex
Labeler / ManufacturerSandoz Inc
Marketing categoryAbbreviated NDA (generic) · App ANDA214311
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsSUGAMMADEX SODIUM (200 mg/2mL)
Marketing started20260728
Package count1

External sources

Source: openFDA. Public-domain (CC0).