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Perforomist - 49502-605-61 - (formoterol fumarate dihydrate)

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Drug Information of Perforomist

Product NDC: 49502-605
Proprietary Name: Perforomist
Non Proprietary Name: formoterol fumarate dihydrate
Active Ingredient(s): 20    ug/2mL & nbsp;   formoterol fumarate dihydrate
Administration Route(s): RESPIRATORY (INHALATION)
Dosage Form(s): SOLUTION
Coding System: National Drug Codes(NDC)

Labeler Information of Perforomist

Product NDC: 49502-605
Labeler Name: Mylan Specialty
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA022007
Marketing Category: NDA
Start Marketing Date: 20070511

Package Information of Perforomist

Package NDC: 49502-605-61
Package Description: 60 POUCH in 1 CARTON (49502-605-61) > 1 VIAL in 1 POUCH > 2 mL in 1 VIAL

NDC Information of Perforomist

NDC Code 49502-605-61
Proprietary Name Perforomist
Package Description 60 POUCH in 1 CARTON (49502-605-61) > 1 VIAL in 1 POUCH > 2 mL in 1 VIAL
Product NDC 49502-605
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name formoterol fumarate dihydrate
Dosage Form Name SOLUTION
Route Name RESPIRATORY (INHALATION)
Start Marketing Date 20070511
Marketing Category Name NDA
Labeler Name Mylan Specialty
Substance Name FORMOTEROL FUMARATE DIHYDRATE
Strength Number 20
Strength Unit ug/2mL
Pharmaceutical Classes Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]

Complete Information of Perforomist


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