# Sugammadex

NDC: 70710-1651
Generic name: Sugammadex
Labeler / Manufacturer: Zydus Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20260702

FDA application: ANDA214290

## 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:"70710-1651"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70710-1651
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=21028965-598b-4cfa-a614-5c28ed40306a