# Fentanyl Citrate

NDC: 0409-9094
Generic name: FENTANYL CITRATE
Labeler / Manufacturer: Hospira, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20050927

FDA application: NDA019115

## Active ingredients

- FENTANYL CITRATE: 50 ug/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0409-9094"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0409-9094
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bfa8018a-4cbc-434b-e09e-782872b0340a