# Fentanyl Citrate

NDC: 0641-6290
Generic name: Fentanyl Citrate
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION
Routes: INTRAVENOUS
Marketing started: 20250829

FDA application: NDA019101

## 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:"0641-6290"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0641-6290
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c5fcdcbd-1dd1-4ebf-aa0d-edfe845414b7