FLUTICASONE PROPIONATE AND SALMETEROL XINAFOATE
FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE
Approval overview FLUTICASONE PROPIONATE AND SALMETEROL XINAFOATE is listed in Drugs@FDA under application 214464 (ANDA).
Review priority: STANDARD Marketing status: Discontinued Active ingredient FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE Form and strength POWDER;INHALATION - 0.25MG/INH;EQ 0.05MG BASE/INH Sponsor RESPIRENT PHARMS Submission history Latest submission status date: 2026-01-12 00:00:00.
Structured Monograph
Clinical summary
Approval overview FLUTICASONE PROPIONATE AND SALMETEROL XINAFOATE is listed in Drugs@FDA under application 214464 (ANDA). Review priority: STANDARD Marketing status: Discontinued Active ingredient FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE Form and strength POWDER;INHALATION - 0.25MG/INH;EQ 0.05MG BASE/INH Sponsor RESPIRENT PHARMS Submission history Latest submission status date: 2026-01-12 00:00:00. Submission type: ORIG.
Monitoring
- • Marketing status: Discontinued
- • Review priority: STANDARD
Interaction Notes
- No interaction notes stored yet.