FDA NDC Directory · JSON-LD · Markdown

Sugammadex

NDC 0641-6270 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerHikma Pharmaceuticals USA Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA218727
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsSUGAMMADEX SODIUM (100 mg/mL)
Marketing started20260728
Package count1

External sources

Source: openFDA. Public-domain (CC0).