FDA NDC Directory · JSON-LD · Markdown

sugammadex

NDC 68462-696 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerGLENMARK PHARMACEUTICALS INC., USA
Marketing categoryAbbreviated NDA (generic) · App ANDA214364
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsSUGAMMADEX SODIUM (500 mg/5mL)
Marketing started20260728
Package count1

External sources

Source: openFDA. Public-domain (CC0).