Product NDC: | 66993-024 |
Proprietary Name: | Fluticasone Propionate |
Non Proprietary Name: | fluticasone propionate |
Active Ingredient(s): | 50 ug/1 & nbsp; fluticasone propionate |
Administration Route(s): | NASAL |
Dosage Form(s): | SPRAY, METERED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 66993-024 |
Labeler Name: | Prasco Laboratories |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020121 |
Marketing Category: | NDA AUTHORIZED GENERIC |
Start Marketing Date: | 20121019 |
Package NDC: | 66993-024-52 |
Package Description: | 1 BOTTLE in 1 CARTON (66993-024-52) > 120 SPRAY, METERED in 1 BOTTLE |
NDC Code | 66993-024-52 |
Proprietary Name | Fluticasone Propionate |
Package Description | 1 BOTTLE in 1 CARTON (66993-024-52) > 120 SPRAY, METERED in 1 BOTTLE |
Product NDC | 66993-024 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | fluticasone propionate |
Dosage Form Name | SPRAY, METERED |
Route Name | NASAL |
Start Marketing Date | 20121019 |
Marketing Category Name | NDA AUTHORIZED GENERIC |
Labeler Name | Prasco Laboratories |
Substance Name | FLUTICASONE PROPIONATE |
Strength Number | 50 |
Strength Unit | ug/1 |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |