# Sugammadex

NDC: 31722-254
Generic name: Sugammadex
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20260727

FDA application: ANDA214337

## Active ingredients

- SUGAMMADEX SODIUM: 100 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"31722-254"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-254
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9adda802-fab2-40c1-9c2f-358debdfb249