# SUGAMMADEX SODIUM

NDC: 42023-935
Generic name: SUGAMMADEX SODIUM
Labeler / Manufacturer: Par Health USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: INTRAVENOUS
Marketing started: 20260728

FDA application: ANDA218814

## 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:"42023-935"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42023-935
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=579a2a1f-4d0c-4851-e063-6294a90a2be6