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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
SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE 0054-0327-56  Hikma Pharmaceuticals USA Inc.  ANDA203433  HUMAN PRESCRIPTION DRUG  ANDA 
FLUTICASONE PROPIONATE 57483-005-03  Innovus Pharmaceuticals Inc.  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 30142-258-04  Kroger Company  ANDA208150  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 30142-258-01  Kroger Company  ANDA208150  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 30142-258-02  Kroger Company  ANDA208150  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 30142-258-05  Kroger Company  ANDA208150  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 30142-258-03  Kroger Company  ANDA208150  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 0113-0028-01  L. Perrigo Company  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 0113-0285-08  L. Perrigo Company  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 0113-0028-02  L. Perrigo Company  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 0113-0285-02  L. Perrigo Company  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 0113-0028-09  L. Perrigo Company  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 0113-0028-08  L. Perrigo Company  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 55700-680-16  Lake Erie Medical DBA Quality Care Products LLC  ANDA078492  HUMAN PRESCRIPTION DRUG  ANDA 
FLUTICASONE PROPIONATE 72559-002-01  Little Pharma, Inc.  ANDA208150  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 80267-000-09  Live Betr LLC  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 80267-000-01  Live Betr LLC  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 68998-600-01  Marc Glassman, Inc.  ANDA208150  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 68998-600-02  Marc Glassman, Inc.  ANDA208150  HUMAN OTC DRUG  ANDA 
AZELASTINE HYDROCHLORIDE; FLUTICASONE PROPIONATE 0037-0245-23  Meda Pharmaceuticals Inc.  NDA202236  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 41250-634-10  Meijer Distribution Inc  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 41250-634-03  Meijer Distribution Inc  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 41250-634-08  Meijer Distribution Inc  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 41250-634-01  Meijer Distribution Inc  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 41250-634-02  Meijer Distribution Inc  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 41250-634-09  Meijer Distribution Inc  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 60432-264-15  Morton Grove Pharmaceuticals, Inc.  ANDA078492  HUMAN PRESCRIPTION DRUG  ANDA 
AZELASTINE HYDROCHLORIDE; FLUTICASONE PROPIONATE 0378-3458-23  Mylan Pharmaceuticals Inc.  NDA202236  HUMAN PRESCRIPTION DRUG  NDA authorized generic 
FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 0378-9322-32  Mylan Pharmaceuticals Inc.  ANDA208891  HUMAN PRESCRIPTION DRUG  ANDA 
SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE 0378-9321-32  Mylan Pharmaceuticals Inc.  ANDA208891  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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