Product NDC: | 0487-9901 |
Proprietary Name: | Albuterol Sulfate |
Non Proprietary Name: | Albuterol Sulfate |
Active Ingredient(s): | 2.5 mg/.5mL & nbsp; Albuterol Sulfate |
Administration Route(s): | RESPIRATORY (INHALATION) |
Dosage Form(s): | SOLUTION |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 0487-9901 |
Labeler Name: | Nephron Pharmaceuticals Corporation |
Product Type: | HUMAN PRESCRIPTION DRUG |
FDA Application Number: | ANDA075664 |
Marketing Category: | ANDA |
Start Marketing Date: | 20010626 |
Package NDC: | 0487-9901-02 |
Package Description: | 30 BAG in 1 BOX (0487-9901-02) > 1 POUCH in 1 BAG > 1 VIAL, SINGLE-DOSE in 1 POUCH > .5 mL in 1 VIAL, SINGLE-DOSE |
NDC Code | 0487-9901-02 |
Proprietary Name | Albuterol Sulfate |
Package Description | 30 BAG in 1 BOX (0487-9901-02) > 1 POUCH in 1 BAG > 1 VIAL, SINGLE-DOSE in 1 POUCH > .5 mL in 1 VIAL, SINGLE-DOSE |
Product NDC | 0487-9901 |
Product Type Name | HUMAN PRESCRIPTION DRUG |
Non Proprietary Name | Albuterol Sulfate |
Dosage Form Name | SOLUTION |
Route Name | RESPIRATORY (INHALATION) |
Start Marketing Date | 20010626 |
Marketing Category Name | ANDA |
Labeler Name | Nephron Pharmaceuticals Corporation |
Substance Name | ALBUTEROL SULFATE |
Strength Number | 2.5 |
Strength Unit | mg/.5mL |
Pharmaceutical Classes | Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC] |