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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 69306-016-01  Doc Rx  ANDA077570  HUMAN PRESCRIPTION DRUG  ANDA 
FLUTICASONE PROPIONATE 55910-773-01  Dolgencorp Inc  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 55910-773-02  Dolgencorp Inc  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 55910-607-02  Dolgencorp, LLC  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 0168-0332-60  E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.  ANDA076451  HUMAN PRESCRIPTION DRUG  ANDA 
FLUTICASONE PROPIONATE 0168-0332-15  E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.  ANDA076451  HUMAN PRESCRIPTION DRUG  ANDA 
FLUTICASONE PROPIONATE 0168-0332-30  E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.  ANDA076451  HUMAN PRESCRIPTION DRUG  ANDA 
FLUTICASONE PROPIONATE 81522-005-02  FSA Store Inc.  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 81522-002-08  FSA Store Inc.  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 81522-073-34  FSA Store Inc. (Caring Mills)  ANDA208024  HUMAN OTC DRUG  ANDA 
SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE 0173-0717-20  GlaxoSmithKline LLC  NDA021254  HUMAN PRESCRIPTION DRUG  NDA 
SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE 0173-0697-00  GlaxoSmithKline LLC  NDA021077  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 0173-0716-22  GlaxoSmithKline LLC  NDA021254  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 0173-0601-02  GlaxoSmithKline LLC  NDA020833  HUMAN PRESCRIPTION DRUG  NDA 
SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE 0173-0697-04  GlaxoSmithKline LLC  NDA021077  HUMAN PRESCRIPTION DRUG  NDA 
SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE 0173-0715-20  GlaxoSmithKline LLC  NDA021254  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 0173-0719-20  GlaxoSmithKline LLC  NDA021433  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 0173-0716-20  GlaxoSmithKline LLC  NDA021254  HUMAN PRESCRIPTION DRUG  NDA 
SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE 0173-0717-22  GlaxoSmithKline LLC  NDA021254  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 0173-0696-04  GlaxoSmithKline LLC  NDA021077  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 0173-0720-20  GlaxoSmithKline LLC  NDA021433  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 0173-0695-04  GlaxoSmithKline LLC  NDA021077  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 0173-0600-02  GlaxoSmithKline LLC  NDA020833  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 0173-0696-00  GlaxoSmithKline LLC  NDA021077  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 0173-0718-20  GlaxoSmithKline LLC  NDA021433  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 0173-0695-00  GlaxoSmithKline LLC  NDA021077  HUMAN PRESCRIPTION DRUG  NDA 
SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE 0173-0715-22  GlaxoSmithKline LLC  NDA021254  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 0173-0602-02  GlaxoSmithKline LLC  NDA020833  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 68462-427-02  Glenmark Pharmaceuticals Inc., USA  ANDA090759  HUMAN PRESCRIPTION DRUG  ANDA 
FLUTICASONE PROPIONATE 60429-195-15  Golden State Medical Supply, Inc.  ANDA077538  HUMAN PRESCRIPTION DRUG  ANDA 
1-30 31-60 61-90 91-120 121-150 151-180 181-210 211-240 241-270 271-300
301-330 331-360 361-390 391-420 421-426

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