# Sugammadex

NDC: 70748-371
Generic name: Sugammadex
Labeler / Manufacturer: Lupin Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20260728

FDA application: ANDA214338

## 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:"70748-371"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70748-371
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9f2e66d7-a5d2-4593-bb30-6d4a418381aa