VENTOLIN - 0173-0682-20 - (albuterol sulfate)

Alphabetical Index


Drug Information of VENTOLIN

Product NDC: 0173-0682
Proprietary Name: VENTOLIN
Non Proprietary Name: albuterol sulfate
Active Ingredient(s): 90    ug/1 & nbsp;   albuterol sulfate
Administration Route(s): RESPIRATORY (INHALATION)
Dosage Form(s): AEROSOL, METERED
Coding System: National Drug Codes(NDC)

Labeler Information of VENTOLIN

Product NDC: 0173-0682
Labeler Name: GlaxoSmithKline LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020983
Marketing Category: NDA
Start Marketing Date: 20060609

Package Information of VENTOLIN

Package NDC: 0173-0682-20
Package Description: 200 AEROSOL, METERED in 1 INHALER (0173-0682-20)

NDC Information of VENTOLIN

NDC Code 0173-0682-20
Proprietary Name VENTOLIN
Package Description 200 AEROSOL, METERED in 1 INHALER (0173-0682-20)
Product NDC 0173-0682
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name albuterol sulfate
Dosage Form Name AEROSOL, METERED
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 20060609
Marketing Category Name NDA
Labeler Name GlaxoSmithKline LLC
Substance Name ALBUTEROL SULFATE
Strength Number 90
Strength Unit ug/1
Pharmaceutical Classes Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]

Complete Information of VENTOLIN


General Information