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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; SALMETEROL XINAFOATE 50090-3271-0  A-S Medication Solutions  NDA208799  HUMAN PRESCRIPTION DRUG  NDA authorized generic 
SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE 59310-520-08  Teva Respiratory, LLC  NDA208799  HUMAN PRESCRIPTION DRUG  NDA 
SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE 0093-3607-82  Teva Pharmaceuticals USA, Inc.  NDA208799  HUMAN PRESCRIPTION DRUG  NDA authorized generic 
SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE 59310-822-08  Teva Respiratory, LLC  NDA208799  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 71143-375-01  OptiNose US, Inc.  NDA209022  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 71143-375-99  OptiNose US, Inc.  NDA209022  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 71143-375-98  OptiNose US, Inc.  NDA209022  HUMAN PRESCRIPTION DRUG  NDA 
1-30 31-60 61-90 91-120 121-150 151-180 181-210 211-240 241-270 271-300
301-330 331-360 361-390 391-420 421-427

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