# Sugammadex

NDC: 0264-8200
Generic name: Sugammadex
Labeler / Manufacturer: B. Braun Medical Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20260728

FDA application: ANDA214279

## Active ingredients

- SUGAMMADEX SODIUM: 200 mg/2mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0264-8200"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0264-8200
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d9d4467c-97ae-462a-9722-cc8d62db3e83