PROAIRHFA - 49349-745-01 - (albuterol sulfate)

Alphabetical Index


Drug Information of PROAIRHFA

Product NDC: 49349-745
Proprietary Name: PROAIRHFA
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 PROAIRHFA

Product NDC: 49349-745
Labeler Name: REMEDYREPACK INC.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021457
Marketing Category: NDA
Start Marketing Date: 20130613

Package Information of PROAIRHFA

Package NDC: 49349-745-01
Package Description: 1 AEROSOL, METERED in 1 CONTAINER (49349-745-01)

NDC Information of PROAIRHFA

NDC Code 49349-745-01
Proprietary Name PROAIRHFA
Package Description 1 AEROSOL, METERED in 1 CONTAINER (49349-745-01)
Product NDC 49349-745
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name albuterol sulfate
Dosage Form Name AEROSOL, METERED
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 20130613
Marketing Category Name NDA
Labeler Name REMEDYREPACK INC.
Substance Name ALBUTEROL SULFATE
Strength Number 90
Strength Unit ug/1
Pharmaceutical Classes Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]

Complete Information of PROAIRHFA


General Information