# sugammadex

NDC: 72266-269
Generic name: sugammadex
Labeler / Manufacturer: Fosun Pharma USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20260729

FDA application: ANDA214364

## Active ingredients

- SUGAMMADEX SODIUM: 500 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72266-269"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72266-269
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4f1c7cf8-3db7-3f92-e063-6394a90aece9