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 |
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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 |
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