# fluticasone propionate and salmeterol

NDC: 0093-7516
Generic name: fluticasone propionate and salmeterol
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER
Routes: RESPIRATORY (INHALATION)
Marketing started: 20220323

FDA application: ANDA213948

## Active ingredients

- FLUTICASONE PROPIONATE: 500 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:"0093-7516"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0093-7516
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ce347bf4-4cc1-46dc-b5f1-6f8ff48da84b