# FLUTICASONE PROPIONATE AND SALMETEROL XINAFOATE
> **ANDA213948** · Abbreviated New Drug Application (Generic) · Sponsor: TEVA PHARMS USA · Approved 2021-12-13
## Drug
- **FDA Application Number:** ANDA213948
- **Application type:** Abbreviated New Drug Application (Generic)
- **Brand name:** FLUTICASONE PROPIONATE AND SALMETEROL XINAFOATE
- **Generic name:** FLUTICASONE PROPIONATE AND SALMETEROL
- **Active ingredients:** FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE
- **Dosage form:** POWDER
- **Route:** INHALATION
- **Marketing status:** Prescription
- **Sponsor:** TEVA PHARMS USA
- **Manufacturer:** Teva Pharmaceuticals USA, Inc.
- **First approval:** 2021-12-13
## Source
- [Drugs@FDA application overview](https://www.accessdata.fda.gov/scripts/cder/daf/index.cfm?event=overview.process&ApplNo=213948)
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