Albuterol - 0378-0572-01 - (albuterol sulfate)

Alphabetical Index


Drug Information of Albuterol

Product NDC: 0378-0572
Proprietary Name: Albuterol
Non Proprietary Name: albuterol sulfate
Active Ingredient(s): 4    mg/1 & nbsp;   albuterol sulfate
Administration Route(s): ORAL
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Albuterol

Product NDC: 0378-0572
Labeler Name: Mylan Pharmaceuticals Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA072894
Marketing Category: ANDA
Start Marketing Date: 20120214

Package Information of Albuterol

Package NDC: 0378-0572-01
Package Description: 100 TABLET in 1 BOTTLE, PLASTIC (0378-0572-01)

NDC Information of Albuterol

NDC Code 0378-0572-01
Proprietary Name Albuterol
Package Description 100 TABLET in 1 BOTTLE, PLASTIC (0378-0572-01)
Product NDC 0378-0572
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name albuterol sulfate
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120214
Marketing Category Name ANDA
Labeler Name Mylan Pharmaceuticals Inc.
Substance Name ALBUTEROL SULFATE
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]

Complete Information of Albuterol


General Information