Product NDC: | 54868-6021 |
Proprietary Name: | Xopenex |
Non Proprietary Name: | levalbuterol hydrochloride |
Active Ingredient(s): | 1.25 mg/.5mL & nbsp; levalbuterol hydrochloride |
Administration Route(s): | RESPIRATORY (INHALATION) |
Dosage Form(s): | SOLUTION, CONCENTRATE |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 54868-6021 |
Labeler Name: | Physicians Total Care, Inc. |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | NDA020837 |
Marketing Category: | NDA |
Start Marketing Date: | 20090421 |
Package NDC: | 54868-6021-0 |
Package Description: | 30 POUCH in 1 CARTON (54868-6021-0) > 1 VIAL in 1 POUCH > .5 mL in 1 VIAL |
NDC Code | 54868-6021-0 |
Proprietary Name | Xopenex |
Package Description | 30 POUCH in 1 CARTON (54868-6021-0) > 1 VIAL in 1 POUCH > .5 mL in 1 VIAL |
Product NDC | 54868-6021 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | levalbuterol hydrochloride |
Dosage Form Name | SOLUTION, CONCENTRATE |
Route Name | RESPIRATORY (INHALATION) |
Start Marketing Date | 20090421 |
Marketing Category Name | NDA |
Labeler Name | Physicians Total Care, Inc. |
Substance Name | LEVALBUTEROL HYDROCHLORIDE |
Strength Number | 1.25 |
Strength Unit | mg/.5mL |
Pharmaceutical Classes | Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC] |