# fluticasone propionate and salmeterol

NDC: 70518-4406
Generic name: fluticasone propionate and salmeterol
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER
Routes: RESPIRATORY (INHALATION)
Marketing started: 20250727

FDA application: ANDA203433

## Active ingredients

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

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-4406"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-4406
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7fdaa6db-82bd-4941-be11-ee80a0784d55