FDA NDC Directory · JSON-LD · Markdown

Sugammadex

NDC 31722-254 · HUMAN PRESCRIPTION DRUG · INJECTION

Labeler / ManufacturerCamber Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA214337
Dosage form / routeINJECTION · INTRAVENOUS
Active ingredientsSUGAMMADEX SODIUM (100 mg/mL)
Marketing started20260727
Package count1

External sources

Source: openFDA. Public-domain (CC0).