Product NDC: | 21695-423 |
Proprietary Name: | VENTOLINHFA |
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: | 21695-423 |
Labeler Name: | Rebel Distributors Corp. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020983 |
Marketing Category: | NDA |
Start Marketing Date: | 20060609 |
Package NDC: | 21695-423-08 |
Package Description: | 60 AEROSOL, METERED in 1 INHALER (21695-423-08) |
NDC Code | 21695-423-08 |
Proprietary Name | VENTOLINHFA |
Package Description | 60 AEROSOL, METERED in 1 INHALER (21695-423-08) |
Product NDC | 21695-423 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | albuterol sulfate |
Dosage Form Name | AEROSOL, METERED |
Route Name | RESPIRATORY (INHALATION) |
Start Marketing Date | 20060609 |
Marketing Category Name | NDA |
Labeler Name | Rebel Distributors Corp. |
Substance Name | ALBUTEROL SULFATE |
Strength Number | 108 |
Strength Unit | ug/1 |
Pharmaceutical Classes | Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC] |