# sugammadex

NDC: 70069-892
Generic name: sugammadex
Labeler / Manufacturer: Somerset Therapeutics, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20260728

FDA application: ANDA215260

## Active ingredients

- SUGAMMADEX SODIUM: 100 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70069-892"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70069-892
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=70c00636-d4ba-4939-802c-9d5a92435c93