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 | 68071-4868-5 | NuCare Pharmaceuticals,Inc. | ANDA076504 | HUMAN PRESCRIPTION DRUG | ANDA |
| FLUTICASONE PROPIONATE | 50383-700-09 | Akorn | ANDA077570 | HUMAN PRESCRIPTION DRUG | ANDA |
| FLUTICASONE PROPIONATE | 50090-2267-0 | A-S Medication Solutions | ANDA077538 | HUMAN PRESCRIPTION DRUG | ANDA |
| FLUTICASONE PROPIONATE | 63187-806-16 | Proficient Rx LP | ANDA076504 | HUMAN PRESCRIPTION DRUG | ANDA |
| FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE | 0173-0717-20 | GlaxoSmithKline LLC | NDA021254 | HUMAN PRESCRIPTION DRUG | NDA |
| FLUTICASONE PROPIONATE; SALMETEROL XINAFOATE | 59310-510-08 | Teva Respiratory, LLC | NDA208799 | HUMAN PRESCRIPTION DRUG | NDA |
| SALMETEROL XINAFOATE; FLUTICASONE PROPIONATE | 59310-822-06 | Teva Respiratory, LLC | NDA208799 | HUMAN PRESCRIPTION DRUG | NDA |
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| 301-330 | 331-360 | 361-390 | 391-420 | 421-427 |
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