# Sugammadex

NDC: 0781-3468
Generic name: sugammadex
Labeler / Manufacturer: Sandoz Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20260728

FDA application: ANDA214311

## Active ingredients

- SUGAMMADEX SODIUM: 200 mg/2mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0781-3468"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0781-3468
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6cf43d88-d410-439e-a2e5-e31086f14fc2