AccuNeb - 49502-692-03 - (albuterol sulfate)

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Drug Information of AccuNeb

Product NDC: 49502-692
Proprietary Name: AccuNeb
Non Proprietary Name: albuterol sulfate
Active Ingredient(s): .63    mg/3mL & nbsp;   albuterol sulfate
Administration Route(s): RESPIRATORY (INHALATION)
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of AccuNeb

Product NDC: 49502-692
Labeler Name: Dey Pharma, LP
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020949
Marketing Category: NDA
Start Marketing Date: 20110210

Package Information of AccuNeb

Package NDC: 49502-692-03
Package Description: 5 POUCH in 1 CARTON (49502-692-03) > 5 VIAL in 1 POUCH > 3 mL in 1 VIAL

NDC Information of AccuNeb

NDC Code 49502-692-03
Proprietary Name AccuNeb
Package Description 5 POUCH in 1 CARTON (49502-692-03) > 5 VIAL in 1 POUCH > 3 mL in 1 VIAL
Product NDC 49502-692
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name albuterol sulfate
Dosage Form Name SOLUTION
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 20110210
Marketing Category Name NDA
Labeler Name Dey Pharma, LP
Substance Name ALBUTEROL SULFATE
Strength Number .63
Strength Unit mg/3mL
Pharmaceutical Classes Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]

Complete Information of AccuNeb


General Information