Home > National Drug Code (NDC) > Albuterol Sulfate

Albuterol Sulfate - 0093-0661-16 - (Albuterol Sulfate)

Alphabetical Index


Drug Information of Albuterol Sulfate

Product NDC: 0093-0661
Proprietary Name: Albuterol Sulfate
Non Proprietary Name: Albuterol Sulfate
Active Ingredient(s): 2    mg/5mL & nbsp;   Albuterol Sulfate
Administration Route(s): ORAL
Dosage Form(s): SYRUP
Coding System: National Drug Codes(NDC)

Labeler Information of Albuterol Sulfate

Product NDC: 0093-0661
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA073419
Marketing Category: ANDA
Start Marketing Date: 19920501

Package Information of Albuterol Sulfate

Package NDC: 0093-0661-16
Package Description: 473 mL in 1 BOTTLE (0093-0661-16)

NDC Information of Albuterol Sulfate

NDC Code 0093-0661-16
Proprietary Name Albuterol Sulfate
Package Description 473 mL in 1 BOTTLE (0093-0661-16)
Product NDC 0093-0661
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Albuterol Sulfate
Dosage Form Name SYRUP
Route Name ORAL
Start Marketing Date 19920501
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name ALBUTEROL SULFATE
Strength Number 2
Strength Unit mg/5mL
Pharmaceutical Classes Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]

Complete Information of Albuterol Sulfate


General Information