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Levalbuterol - 0093-4148-64 - (Levalbuterol)

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Drug Information of Levalbuterol

Product NDC: 0093-4148
Proprietary Name: Levalbuterol
Non Proprietary Name: Levalbuterol
Active Ingredient(s): 1.25    mg/3mL & nbsp;   Levalbuterol
Administration Route(s): RESPIRATORY (INHALATION)
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Levalbuterol

Product NDC: 0093-4148
Labeler Name: Teva Pharmaceuticals USA Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090297
Marketing Category: ANDA
Start Marketing Date: 20130426

Package Information of Levalbuterol

Package NDC: 0093-4148-64
Package Description: 6 POUCH in 1 CARTON (0093-4148-64) > 4 VIAL, SINGLE-DOSE in 1 POUCH (0093-4148-04) > 3 mL in 1 VIAL, SINGLE-DOSE

NDC Information of Levalbuterol

NDC Code 0093-4148-64
Proprietary Name Levalbuterol
Package Description 6 POUCH in 1 CARTON (0093-4148-64) > 4 VIAL, SINGLE-DOSE in 1 POUCH (0093-4148-04) > 3 mL in 1 VIAL, SINGLE-DOSE
Product NDC 0093-4148
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Levalbuterol
Dosage Form Name SOLUTION
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 20130426
Marketing Category Name ANDA
Labeler Name Teva Pharmaceuticals USA Inc
Substance Name LEVALBUTEROL HYDROCHLORIDE
Strength Number 1.25
Strength Unit mg/3mL
Pharmaceutical Classes Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]

Complete Information of Levalbuterol


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