# Fluticasone Propionate and Salmeterol

NDC: 0527-6010
Generic name: fluticasone propionate and salmeterol
Labeler / Manufacturer: Lannett Company, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER
Routes: RESPIRATORY (INHALATION)
Marketing started: 20260112

FDA application: ANDA214464

## Active ingredients

- FLUTICASONE PROPIONATE: 100 ug/1
- SALMETEROL XINAFOATE: 50 ug/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0527-6010"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0527-6010
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9c1680db-16e9-4658-977b-110631f95a65