| 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: | 75989-550-63 |
| Package Description: | 1 INHALER in 1 CARTON (75989-550-63) > 60 AEROSOL, METERED in 1 INHALER |
| NDC Code | 75989-550-63 |
| Proprietary Name | Aerospan |
| Package Description | 1 INHALER in 1 CARTON (75989-550-63) > 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] |