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U.S. Department of Health and Human Services

FDA Application

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NDC Search Results on Active Ingredient: fluticasone propionate

Click on Active Ingredient to view the label.

Ingredient Name NDC Company Name Application Number or Regulatory Citation Product Type Marketing Category
FLUTICASONE PROPIONATE 0135-0576-12  Haleon US Holdings LLC  NDA205434  HUMAN OTC DRUG  NDA 
FLUTICASONE PROPIONATE 0135-0582-03  Haleon US Holdings LLC  NDA205434  HUMAN OTC DRUG  NDA 
FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 0173-0696-00  GlaxoSmithKline LLC  NDA021077  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 0135-0576-04  Haleon US Holdings LLC  NDA205434  HUMAN OTC DRUG  NDA 
SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE 59310-520-08  Teva Respiratory, LLC  NDA208799  HUMAN PRESCRIPTION DRUG  NDA 
SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE 68258-3031-1  Dispensing Solutions, Inc.  NDA021077  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE; AZELASTINE HYDROCHLORIDE 0037-0245-23  Meda Pharmaceuticals Inc.  NDA202236  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 0173-0696-04  GlaxoSmithKline LLC  NDA021077  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 0173-0716-20  GlaxoSmithKline LLC  NDA021254  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 0173-0695-00  GlaxoSmithKline LLC  NDA021077  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 50090-0731-0  A-S Medication Solutions  NDA021077  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 0173-0715-22  GlaxoSmithKline LLC  NDA021254  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 0135-0576-18  Haleon US Holdings LLC  NDA205434  HUMAN OTC DRUG  NDA 
FLUTICASONE PROPIONATE 0173-0718-20  GlaxoSmithKline LLC  NDA021433  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 71143-375-01  OptiNose US, Inc.  NDA209022  HUMAN PRESCRIPTION DRUG  NDA 
SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE 33261-874-01  Aidarex Pharmaceuticals LLC  NDA021077  HUMAN PRESCRIPTION DRUG  NDA 
SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE 21695-361-60  Rebel Distributors Corp.  NDA021077  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 0135-0576-02  Haleon US Holdings LLC  NDA205434  HUMAN OTC DRUG  NDA 
SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE 0173-0697-04  GlaxoSmithKline LLC  NDA021077  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 59310-505-08  Teva Respiratory, LLC  NDA208798  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 21695-197-01  Rebel Distributors Corp.  NDA021077  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 50090-0934-0  A-S Medication Solutions  NDA021433  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 50090-1245-0  A-S Medication Solutions  NDA020833  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 0135-0576-03  Haleon US Holdings LLC  NDA205434  HUMAN OTC DRUG  NDA 
FLUTICASONE PROPIONATE 66993-791-97  Prasco Laboratories  NDA020833  HUMAN PRESCRIPTION DRUG  NDA authorized generic 
FLUTICASONE PROPIONATE 50090-7076-0  A-S Medication Solutions  NDA020833  HUMAN PRESCRIPTION DRUG  NDA authorized generic 
SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE 66993-585-97  Prasco Laboratories  NDA021077  HUMAN PRESCRIPTION DRUG  NDA authorized generic 
FLUTICASONE PROPIONATE 66993-790-97  Prasco Laboratories  NDA020833  HUMAN PRESCRIPTION DRUG  NDA authorized generic 
SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE 66993-584-97  Prasco Laboratories  NDA021077  HUMAN PRESCRIPTION DRUG  NDA authorized generic 
FLUTICASONE PROPIONATE 66993-080-96  Prasco Laboratories  NDA021433  HUMAN PRESCRIPTION DRUG  NDA authorized generic 
1-30 31-60 61-90 91-120 121-150 151-180 181-210 211-240 241-270 271-300
301-330 331-360 361-390 391-419

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