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albuterol sulfate - 63629-2736-3 - (albuterol sulfate)

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Drug Information of albuterol sulfate

Product NDC: 63629-2736
Proprietary Name: albuterol sulfate
Non Proprietary Name: albuterol sulfate
Active Ingredient(s): 4    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: 63629-2736
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072637
Marketing Category: ANDA
Start Marketing Date: 19891205

Package Information of albuterol sulfate

Package NDC: 63629-2736-3
Package Description: 60 TABLET in 1 BOTTLE (63629-2736-3)

NDC Information of albuterol sulfate

NDC Code 63629-2736-3
Proprietary Name albuterol sulfate
Package Description 60 TABLET in 1 BOTTLE (63629-2736-3)
Product NDC 63629-2736
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 Bryant Ranch Prepack
Substance Name ALBUTEROL SULFATE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]

Complete Information of albuterol sulfate


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