# Sufentanil Citrate

NDC: 0409-3382
Generic name: SUFENTANIL CITRATE
Labeler / Manufacturer: Hospira, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, SOLUTION
Routes: EPIDURAL, INTRAVENOUS
Marketing started: 20050726

FDA application: ANDA074534

## Active ingredients

- SUFENTANIL CITRATE: 50 ug/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0409-3382"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0409-3382
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=20293943-46ff-4345-1aa4-929b4e017a25