PROAIR - 49999-908-85 - (albuterol sulfate)

Alphabetical Index


Drug Information of PROAIR

Product NDC: 49999-908
Proprietary Name: PROAIR
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 PROAIR

Product NDC: 49999-908
Labeler Name: Lake Erie Medical & Surgical Supply DBA Quality Care Products LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021457
Marketing Category: NDA
Start Marketing Date: 20120321

Package Information of PROAIR

Package NDC: 49999-908-85
Package Description: 200 AEROSOL, METERED in 1 INHALER (49999-908-85)

NDC Information of PROAIR

NDC Code 49999-908-85
Proprietary Name PROAIR
Package Description 200 AEROSOL, METERED in 1 INHALER (49999-908-85)
Product NDC 49999-908
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name albuterol sulfate
Dosage Form Name AEROSOL, METERED
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 20120321
Marketing Category Name NDA
Labeler Name Lake Erie Medical & Surgical Supply DBA Quality Care Products 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 PROAIR


General Information