Product NDC: | 49502-692 |
Proprietary Name: | AccuNeb |
Non Proprietary Name: | albuterol sulfate |
Active Ingredient(s): | .63 mg/3mL & nbsp; albuterol sulfate |
Administration Route(s): | RESPIRATORY (INHALATION) |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 49502-692 |
Labeler Name: | Dey Pharma, LP |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020949 |
Marketing Category: | NDA |
Start Marketing Date: | 20110210 |
Package NDC: | 49502-692-03 |
Package Description: | 5 POUCH in 1 CARTON (49502-692-03) > 5 VIAL in 1 POUCH > 3 mL in 1 VIAL |
NDC Code | 49502-692-03 |
Proprietary Name | AccuNeb |
Package Description | 5 POUCH in 1 CARTON (49502-692-03) > 5 VIAL in 1 POUCH > 3 mL in 1 VIAL |
Product NDC | 49502-692 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | albuterol sulfate |
Dosage Form Name | SOLUTION |
Route Name | RESPIRATORY (INHALATION) |
Start Marketing Date | 20110210 |
Marketing Category Name | NDA |
Labeler Name | Dey Pharma, LP |
Substance Name | ALBUTEROL SULFATE |
Strength Number | .63 |
Strength Unit | mg/3mL |
Pharmaceutical Classes | Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC] |