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Albuterol Sulfate - 0781-7155-64 - (Albuterol Sulfate)

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Drug Information of Albuterol Sulfate

Product NDC: 0781-7155
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: 0781-7155
Labeler Name: Sandoz Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077839
Marketing Category: ANDA
Start Marketing Date: 20110817

Package Information of Albuterol Sulfate

Package NDC: 0781-7155-64
Package Description: 1 POUCH in 1 CARTON (0781-7155-64) > 30 AMPULE in 1 POUCH > 3 mL in 1 AMPULE

NDC Information of Albuterol Sulfate

NDC Code 0781-7155-64
Proprietary Name Albuterol Sulfate
Package Description 1 POUCH in 1 CARTON (0781-7155-64) > 30 AMPULE in 1 POUCH > 3 mL in 1 AMPULE
Product NDC 0781-7155
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Albuterol Sulfate
Dosage Form Name SOLUTION
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 20110817
Marketing Category Name ANDA
Labeler Name Sandoz 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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