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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 69842-900-08  CVS Pharmacy  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 30142-258-04  Kroger Company  ANDA208150  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 37835-997-31  Bi-Mart  ANDA208150  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 45802-221-37  Padagis Israel Pharmaceuticals Ltd  ANDA076668  HUMAN PRESCRIPTION DRUG  ANDA 
FLUTICASONE PROPIONATE 68998-600-01  Marc Glassman, Inc.  ANDA208150  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 0363-1205-08  Walgreen Company  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 63654-380-01  Selder, S.A. de C.V.  ANDA208150  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 0113-0028-08  L. Perrigo Company  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 56062-107-08  Publix Super Markets Inc  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 73309-304-01  BLUEBAY SHANDONG CO.,LTD    BULK INGREDIENT  bulk ingredient for animal drug compounding 
FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 59310-805-08  Teva Respiratory, LLC  NDA208799  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 0135-0576-17  Haleon US Holdings LLC  NDA205434  HUMAN OTC DRUG  NDA 
FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 59310-136-06  Teva Respiratory, LLC  NDA208799  HUMAN PRESCRIPTION DRUG  NDA 
SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE 50090-4504-0  A-S Medication Solutions  NDA021254  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 59310-805-06  Teva Respiratory, LLC  NDA208799  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 0173-0720-20  GlaxoSmithKline LLC  NDA021433  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 59310-200-06  Teva Respiratory, LLC  NDA208798  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 0173-0716-22  GlaxoSmithKline LLC  NDA021254  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 50090-1978-0  A-S Medication Solutions  NDA205434  HUMAN OTC DRUG  NDA 
FLUTICASONE PROPIONATE 71143-375-99  OptiNose US, Inc.  NDA209022  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 59310-822-08  Teva Respiratory, LLC  NDA208799  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 76519-1177-0  H.J. Harkins Company, Inc.  NDA020833  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 10337-332-30  PharmaDerm a division of Fougera Pharmaceuticals Inc.  NDA019958  HUMAN PRESCRIPTION DRUG  NDA 
SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE 0173-0697-00  GlaxoSmithKline LLC  NDA021077  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 0135-0582-04  Haleon US Holdings LLC  NDA205434  HUMAN OTC DRUG  NDA 
FLUTICASONE PROPIONATE 0173-0600-02  GlaxoSmithKline LLC  NDA020833  HUMAN PRESCRIPTION DRUG  NDA 
SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE 0173-0717-22  GlaxoSmithKline LLC  NDA021254  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 0135-0576-16  Haleon US Holdings LLC  NDA205434  HUMAN OTC DRUG  NDA 
SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE 59310-530-08  Teva Respiratory, LLC  NDA208799  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE 59310-510-08  Teva Respiratory, LLC  NDA208799  HUMAN PRESCRIPTION DRUG  NDA 
1-30 31-60 61-90 91-120 121-150 151-180 181-210 211-240 241-270 271-300
301-330 331-360 361-390 391-419

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