Product NDC: | 75989-550 |
Proprietary Name: | Aerospan |
Non Proprietary Name: | flunisolide |
Active Ingredient(s): | 80 ug/1 & nbsp; flunisolide |
Administration Route(s): | RESPIRATORY (INHALATION) |
Dosage Form(s): | AEROSOL, METERED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 75989-550 |
Labeler Name: | Acton Pharmaceuticals, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA021247 |
Marketing Category: | NDA |
Start Marketing Date: | 20120301 |
Package NDC: | 75989-550-06 |
Package Description: | 1 INHALER in 1 CARTON (75989-550-06) > 60 AEROSOL, METERED in 1 INHALER |
NDC Code | 75989-550-06 |
Proprietary Name | Aerospan |
Package Description | 1 INHALER in 1 CARTON (75989-550-06) > 60 AEROSOL, METERED in 1 INHALER |
Product NDC | 75989-550 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | flunisolide |
Dosage Form Name | AEROSOL, METERED |
Route Name | RESPIRATORY (INHALATION) |
Start Marketing Date | 20120301 |
Marketing Category Name | NDA |
Labeler Name | Acton Pharmaceuticals, Inc. |
Substance Name | FLUNISOLIDE |
Strength Number | 80 |
Strength Unit | ug/1 |
Pharmaceutical Classes | Corticosteroid [EPC],Corticosteroid Hormone Receptor Agonists [MoA] |