Product NDC: | 49999-907 |
Proprietary Name: | Proventil HFA |
Non Proprietary Name: | Albuterol Sulfate |
Active Ingredient(s): | 108 ug/1 & nbsp; Albuterol Sulfate |
Administration Route(s): | RESPIRATORY (INHALATION) |
Dosage Form(s): | AEROSOL, METERED |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49999-907 |
Labeler Name: | Lake Erie Medical DBA Quality Care Products LLC |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020503 |
Marketing Category: | NDA |
Start Marketing Date: | 20011001 |
Package NDC: | 49999-907-67 |
Package Description: | 1 AEROSOL, METERED in 1 CARTON (49999-907-67) |
NDC Code | 49999-907-67 |
Proprietary Name | Proventil HFA |
Package Description | 1 AEROSOL, METERED in 1 CARTON (49999-907-67) |
Product NDC | 49999-907 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Albuterol Sulfate |
Dosage Form Name | AEROSOL, METERED |
Route Name | RESPIRATORY (INHALATION) |
Start Marketing Date | 20011001 |
Marketing Category Name | NDA |
Labeler Name | Lake Erie Medical DBA Quality Care Products LLC |
Substance Name | ALBUTEROL SULFATE |
Strength Number | 108 |
Strength Unit | ug/1 |
Pharmaceutical Classes | Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC] |