Home > National Drug Code (NDC) > Albuterol Sulfate

Albuterol Sulfate - 54868-3407-0 - (Albuterol Sulfate)

Alphabetical Index


Drug Information of Albuterol Sulfate

Product NDC: 54868-3407
Proprietary Name: Albuterol Sulfate
Non Proprietary Name: Albuterol Sulfate
Active Ingredient(s): 5    mg/mL & nbsp;   Albuterol Sulfate
Administration Route(s): RESPIRATORY (INHALATION)
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Albuterol Sulfate

Product NDC: 54868-3407
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA074543
Marketing Category: ANDA
Start Marketing Date: 19941019

Package Information of Albuterol Sulfate

Package NDC: 54868-3407-0
Package Description: 1 BOTTLE, GLASS in 1 CARTON (54868-3407-0) > 20 mL in 1 BOTTLE, GLASS

NDC Information of Albuterol Sulfate

NDC Code 54868-3407-0
Proprietary Name Albuterol Sulfate
Package Description 1 BOTTLE, GLASS in 1 CARTON (54868-3407-0) > 20 mL in 1 BOTTLE, GLASS
Product NDC 54868-3407
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Albuterol Sulfate
Dosage Form Name SOLUTION
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 19941019
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name ALBUTEROL SULFATE
Strength Number 5
Strength Unit mg/mL
Pharmaceutical Classes Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]

Complete Information of Albuterol Sulfate


General Information