# fluticasone propionate and salmeterol

NDC: 68788-8453
Generic name: fluticasone propionate and salmeterol
Labeler / Manufacturer: Preferred Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: POWDER
Routes: RESPIRATORY (INHALATION)
Marketing started: 20230530

FDA application: ANDA203433

## Active ingredients

- FLUTICASONE PROPIONATE: 250 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:"68788-8453"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-8453
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0dea4818-e9d6-42f2-a702-90419fff2695