# FENTANYL TRANSDERMAL

NDC: 0406-9062
Generic name: fentanyl transdermal
Labeler / Manufacturer: SpecGx LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: PATCH, EXTENDED RELEASE
Routes: TRANSDERMAL
Marketing started: 20200228

FDA application: ANDA077154

## Active ingredients

- FENTANYL: 62.5 ug/h

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0406-9062"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0406-9062
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e15a7e9b-8025-49dd-9a6d-bafcccf1959f