Home > National Drug Code (NDC) > Albuterol Sulfate

Albuterol Sulfate - 76204-200-30 - (Albuterol Sulfate)

Alphabetical Index


Drug Information of Albuterol Sulfate

Product NDC: 76204-200
Proprietary Name: Albuterol Sulfate
Non Proprietary Name: Albuterol Sulfate
Active Ingredient(s): 2.5    mg/3mL & 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: 76204-200
Labeler Name: Ritedose Pharmaceuticals, LLC
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077839
Marketing Category: ANDA
Start Marketing Date: 20111205

Package Information of Albuterol Sulfate

Package NDC: 76204-200-30
Package Description: 1 POUCH in 1 CARTON (76204-200-30) > 30 AMPULE in 1 POUCH > 3 mL in 1 AMPULE

NDC Information of Albuterol Sulfate

NDC Code 76204-200-30
Proprietary Name Albuterol Sulfate
Package Description 1 POUCH in 1 CARTON (76204-200-30) > 30 AMPULE in 1 POUCH > 3 mL in 1 AMPULE
Product NDC 76204-200
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Albuterol Sulfate
Dosage Form Name SOLUTION
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 20111205
Marketing Category Name ANDA
Labeler Name Ritedose Pharmaceuticals, LLC
Substance Name ALBUTEROL SULFATE
Strength Number 2.5
Strength Unit mg/3mL
Pharmaceutical Classes Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]

Complete Information of Albuterol Sulfate


General Information