# sugammadex

NDC: 68083-442
Generic name: sugammadex
Labeler / Manufacturer: Gland Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20260728

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:"68083-442"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68083-442
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c61ee55a-e61b-4d3c-9ebc-cbf57290e36c