FDA NDC Directory · JSON-LD · Markdown

Sugammadex

NDC 70748-370 · HUMAN PRESCRIPTION DRUG · INJECTION, SOLUTION

Labeler / ManufacturerLupin Pharmaceuticals, Inc.
Marketing categoryAbbreviated NDA (generic) · App ANDA214338
Dosage form / routeINJECTION, SOLUTION · INTRAVENOUS
Active ingredientsSUGAMMADEX SODIUM (100 mg/mL)
Marketing started20260728
Package count1

External sources

Source: openFDA. Public-domain (CC0).