Home
>
National Drug Code (NDC)
>
Fluticasone Propionate
Fluticasone Propionate - 21695-704-16 - (Fluticasone Propionate)
Drug Information of Fluticasone Propionate
| Product NDC: | 21695-704 |
| Proprietary Name: | Fluticasone Propionate |
| Non Proprietary Name: | Fluticasone Propionate |
| Active Ingredient(s): | 50 ug/.1g & nbsp; Fluticasone Propionate |
| Administration Route(s): | NASAL |
| Dosage Form(s): | SPRAY, METERED |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Fluticasone Propionate
| Product NDC: | 21695-704 |
| Labeler Name: | Rebel Distributors Corp |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA077570 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20080116 |
Package Information of Fluticasone Propionate
| Package NDC: | 21695-704-16 |
| Package Description: | 1 BOTTLE, PUMP in 1 CARTON (21695-704-16) > 16 g in 1 BOTTLE, PUMP |
NDC Information of Fluticasone Propionate
| NDC Code | 21695-704-16 |
| Proprietary Name | Fluticasone Propionate |
| Package Description | 1 BOTTLE, PUMP in 1 CARTON (21695-704-16) > 16 g in 1 BOTTLE, PUMP |
| Product NDC | 21695-704 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Fluticasone Propionate |
| Dosage Form Name | SPRAY, METERED |
| Route Name | NASAL |
| Start Marketing Date | 20080116 |
| Marketing Category Name | ANDA |
| Labeler Name | Rebel Distributors Corp |
| Substance Name | FLUTICASONE PROPIONATE |
| Strength Number | 50 |
| Strength Unit | ug/.1g |
| Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |
