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Albuterol Sulfate - 0591-3797-60 - (Albuterol Sulfate)

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Drug Information of Albuterol Sulfate

Product NDC: 0591-3797
Proprietary Name: Albuterol Sulfate
Non Proprietary Name: Albuterol Sulfate
Active Ingredient(s): 2.5    mg/3mL & nbsp;   Albuterol Sulfate
Administration Route(s): INTRABRONCHIAL
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Albuterol Sulfate

Product NDC: 0591-3797
Labeler Name: Watson Laboratories, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077839
Marketing Category: ANDA
Start Marketing Date: 20101104

Package Information of Albuterol Sulfate

Package NDC: 0591-3797-60
Package Description: 60 VIAL in 1 CARTON (0591-3797-60) > 3 mL in 1 VIAL

NDC Information of Albuterol Sulfate

NDC Code 0591-3797-60
Proprietary Name Albuterol Sulfate
Package Description 60 VIAL in 1 CARTON (0591-3797-60) > 3 mL in 1 VIAL
Product NDC 0591-3797
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Albuterol Sulfate
Dosage Form Name SOLUTION
Route Name INTRABRONCHIAL
Start Marketing Date 20101104
Marketing Category Name ANDA
Labeler Name Watson Laboratories, Inc.
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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