• Decrease font size
  • Return font size to normal
  • Increase font size
U.S. Department of Health and Human Services

FDA Application

  • Print
  • Share
  • E-mail
-

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 37808-205-09  H E B  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 37808-205-10  H E B  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 37808-340-08  H E B  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 37808-205-03  H E B  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 37808-205-02  H E B  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 37808-205-01  H E B  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 37808-340-02  H E B  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 37808-205-08  H E B  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 76519-1018-5  H J Harkins Company, Inc.  ANDA076793  HUMAN PRESCRIPTION DRUG  ANDA 
FLUTICASONE PROPIONATE 76519-1177-0  H.J. Harkins Company, Inc.  NDA020833  HUMAN PRESCRIPTION DRUG  NDA 
FLUTICASONE PROPIONATE 0135-0576-16  Haleon US Holdings LLC  NDA205434  HUMAN OTC DRUG  NDA 
FLUTICASONE PROPIONATE 0135-0576-17  Haleon US Holdings LLC  NDA205434  HUMAN OTC DRUG  NDA 
FLUTICASONE PROPIONATE 0135-0582-01  Haleon US Holdings LLC  NDA205434  HUMAN OTC DRUG  NDA 
FLUTICASONE PROPIONATE 0135-0576-01  Haleon US Holdings LLC  NDA205434  HUMAN OTC DRUG  NDA 
FLUTICASONE PROPIONATE 0135-0582-02  Haleon US Holdings LLC  NDA205434  HUMAN OTC DRUG  NDA 
FLUTICASONE PROPIONATE 0135-0582-05  Haleon US Holdings LLC  NDA205434  HUMAN OTC DRUG  NDA 
FLUTICASONE PROPIONATE 0135-0576-14  Haleon US Holdings LLC  NDA205434  HUMAN OTC DRUG  NDA 
FLUTICASONE PROPIONATE 0135-0576-15  Haleon US Holdings LLC  NDA205434  HUMAN OTC DRUG  NDA 
FLUTICASONE PROPIONATE 0135-0576-18  Haleon US Holdings LLC  NDA205434  HUMAN OTC DRUG  NDA 
FLUTICASONE PROPIONATE 0135-0576-02  Haleon US Holdings LLC  NDA205434  HUMAN OTC DRUG  NDA 
FLUTICASONE PROPIONATE 0135-0582-04  Haleon US Holdings LLC  NDA205434  HUMAN OTC DRUG  NDA 
FLUTICASONE PROPIONATE 0135-0576-03  Haleon US Holdings LLC  NDA205434  HUMAN OTC DRUG  NDA 
FLUTICASONE PROPIONATE 0135-0576-04  Haleon US Holdings LLC  NDA205434  HUMAN OTC DRUG  NDA 
FLUTICASONE PROPIONATE 0135-0576-12  Haleon US Holdings LLC  NDA205434  HUMAN OTC DRUG  NDA 
FLUTICASONE PROPIONATE 0135-0582-03  Haleon US Holdings LLC  NDA205434  HUMAN OTC DRUG  NDA 
FLUTICASONE PROPIONATE 69256-061-02  Harris Teeter, LLC  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 69256-061-01  Harris Teeter, LLC  ANDA207957  HUMAN OTC DRUG  ANDA 
FLUTICASONE PROPIONATE 0054-3270-99  Hikma Pharmaceuticals USA Inc.  ANDA076504  HUMAN PRESCRIPTION DRUG  ANDA 
SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE 0054-0328-56  Hikma Pharmaceuticals USA Inc.  ANDA203433  HUMAN PRESCRIPTION DRUG  ANDA 
SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE 0054-0326-56  Hikma Pharmaceuticals USA Inc.  ANDA203433  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

Return to the FDA Label Search Page

-
-