# Sugammadex

NDC: 43598-924
Generic name: Sugammadex
Labeler / Manufacturer: Dr. Reddy's Laboratories Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: INTRAVENOUS
Marketing started: 20260728

FDA application: ANDA214236

## Active ingredients

- SUGAMMADEX SODIUM: 200 mg/2mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43598-924"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-924
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4f90c37e-3505-0968-38fd-fc7e4dd66e82