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albuterol sulfate - 53489-176-01 - (albuterol sulfate)

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Drug Information of albuterol sulfate

Product NDC: 53489-176
Proprietary Name: albuterol sulfate
Non Proprietary Name: albuterol sulfate
Active Ingredient(s): 2    mg/1 & nbsp;   albuterol sulfate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of albuterol sulfate

Product NDC: 53489-176
Labeler Name: Mutual Pharmaceutical Company, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072637
Marketing Category: ANDA
Start Marketing Date: 19891205

Package Information of albuterol sulfate

Package NDC: 53489-176-01
Package Description: 100 TABLET in 1 BOTTLE (53489-176-01)

NDC Information of albuterol sulfate

NDC Code 53489-176-01
Proprietary Name albuterol sulfate
Package Description 100 TABLET in 1 BOTTLE (53489-176-01)
Product NDC 53489-176
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name albuterol sulfate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 19891205
Marketing Category Name ANDA
Labeler Name Mutual Pharmaceutical Company, Inc.
Substance Name ALBUTEROL SULFATE
Strength Number 2
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]

Complete Information of albuterol sulfate


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