PROAIR - 21695-851-85 - (albuterol sulfate)

Alphabetical Index


Drug Information of PROAIR

Product NDC: 21695-851
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: 21695-851
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021457
Marketing Category: NDA
Start Marketing Date: 19810101

Package Information of PROAIR

Package NDC: 21695-851-85
Package Description: 200 AEROSOL, METERED in 1 INHALER (21695-851-85)

NDC Information of PROAIR

NDC Code 21695-851-85
Proprietary Name PROAIR
Package Description 200 AEROSOL, METERED in 1 INHALER (21695-851-85)
Product NDC 21695-851
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name albuterol sulfate
Dosage Form Name AEROSOL, METERED
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 19810101
Marketing Category Name NDA
Labeler Name Rebel Distributors Corp
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