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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 50090-1187-0  A-S Medication Solutions  ANDA076793  HUMAN PRESCRIPTION DRUG  ANDA 
SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE 50090-0731-0  A-S Medication Solutions  NDA021077  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 0173-0716-22  GlaxoSmithKline LLC  NDA021254  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE; AZELASTINE HYDROCHLORIDE 72162-2127-2  Bryant Ranch Prepack  ANDA207712  HUMAN PRESCRIPTION DRUG  ANDA 
FLUTICASONE PROPIONATE 0173-0601-02  GlaxoSmithKline LLC  NDA020833  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 59310-525-08  Teva Respiratory, LLC  NDA208798  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 0713-0631-15  Cosette Pharmaceuticals, Inc.  ANDA077055  HUMAN PRESCRIPTION DRUG  ANDA 
FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 0378-9322-32  Mylan Pharmaceuticals Inc.  ANDA208891  HUMAN PRESCRIPTION DRUG  ANDA 
FLUTICASONE PROPIONATE 50090-0910-0  A-S Medication Solutions  NDA021433  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 0168-0332-15  E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.  ANDA076451  HUMAN PRESCRIPTION DRUG  ANDA 
FLUTICASONE PROPIONATE 0713-0632-60  Cosette Pharmaceuticals, Inc.  ANDA077168  HUMAN PRESCRIPTION DRUG  ANDA 
FLUTICASONE PROPIONATE 63629-8658-1  Bryant Ranch Prepack  ANDA076793  HUMAN PRESCRIPTION DRUG  ANDA 
FLUTICASONE PROPIONATE 21695-704-16  Rebel Distributors Corp.  ANDA077570  HUMAN PRESCRIPTION DRUG  ANDA 
SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE 0173-0697-00  GlaxoSmithKline LLC  NDA021077  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 50090-0968-0  A-S Medication Solutions  ANDA077538  HUMAN PRESCRIPTION DRUG  ANDA 
FLUTICASONE PROPIONATE 68788-8446-1  Preferred Pharmaceuticals Inc.  ANDA076504  HUMAN PRESCRIPTION DRUG  ANDA 
FLUTICASONE PROPIONATE 0713-0631-31  Cosette Pharmaceuticals, Inc.  ANDA077055  HUMAN PRESCRIPTION DRUG  ANDA 
FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 0093-7517-31  Teva Pharmaceuticals USA, Inc.  ANDA213948  HUMAN PRESCRIPTION DRUG  ANDA 
FLUTICASONE PROPIONATE 51672-4095-3  Taro Pharmaceuticals U.S.A., Inc.  ANDA077145  HUMAN PRESCRIPTION DRUG  ANDA 
FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 59310-812-08  Teva Respiratory, LLC  NDA208799  HUMAN PRESCRIPTION DRUG  NDA 
SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE 0378-9321-32  Mylan Pharmaceuticals Inc.  ANDA208891  HUMAN PRESCRIPTION DRUG  ANDA 
SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE 0173-0717-20  GlaxoSmithKline LLC  NDA021254  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 50090-4504-0  A-S Medication Solutions  NDA021254  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 63629-8661-1  Bryant Ranch Prepack  ANDA076668  HUMAN PRESCRIPTION DRUG  ANDA 
FLUTICASONE PROPIONATE 10544-653-99  Blenheim Pharmacal, Inc.  ANDA077538  HUMAN PRESCRIPTION DRUG  ANDA 
FLUTICASONE PROPIONATE 63629-8660-1  Bryant Ranch Prepack  ANDA076793  HUMAN PRESCRIPTION DRUG  ANDA 
SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE 0173-0697-04  GlaxoSmithKline LLC  NDA021077  HUMAN PRESCRIPTION DRUG  NDA 
SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE 0093-3609-82  Teva Pharmaceuticals USA, Inc.  NDA208799  HUMAN PRESCRIPTION DRUG  NDA authorized generic 
FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 50090-4213-0  A-S Medication Solutions  NDA021077  HUMAN PRESCRIPTION DRUG  NDA authorized generic 
FLUTICASONE PROPIONATE 0168-0332-30  E. Fougera & Co. a division of Fougera Pharmaceuticals Inc.  ANDA076451  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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