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Albuterol Sulfate - 0487-9501-02 - (Albuterol Sulfate)

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Drug Information of Albuterol Sulfate

Product NDC: 0487-9501
Proprietary Name: Albuterol Sulfate
Non Proprietary Name: Albuterol Sulfate
Active Ingredient(s): 2.5    mg/3mL & nbsp;   Albuterol Sulfate
Administration Route(s): RESPIRATORY (INHALATION)
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Albuterol Sulfate

Product NDC: 0487-9501
Labeler Name: Nephron Pharmaceuticals Corporation
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074880
Marketing Category: ANDA
Start Marketing Date: 19970917

Package Information of Albuterol Sulfate

Package NDC: 0487-9501-02
Package Description: 30 BAG in 1 BOX (0487-9501-02) > 1 POUCH in 1 BAG > 1 VIAL, SINGLE-DOSE in 1 POUCH > 3 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Albuterol Sulfate

NDC Code 0487-9501-02
Proprietary Name Albuterol Sulfate
Package Description 30 BAG in 1 BOX (0487-9501-02) > 1 POUCH in 1 BAG > 1 VIAL, SINGLE-DOSE in 1 POUCH > 3 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0487-9501
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Albuterol Sulfate
Dosage Form Name SOLUTION
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 19970917
Marketing Category Name ANDA
Labeler Name Nephron Pharmaceuticals Corporation
Substance Name ALBUTEROL SULFATE
Strength Number 2.5
Strength Unit mg/3mL
Pharmaceutical Classes Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]

Complete Information of Albuterol Sulfate


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