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ZAFIRLUKAST - 49884-304-02 - (Zafirlukast)

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Drug Information of ZAFIRLUKAST

Product NDC: 49884-304
Proprietary Name: ZAFIRLUKAST
Non Proprietary Name: Zafirlukast
Active Ingredient(s): 20    mg/1 & nbsp;   Zafirlukast
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of ZAFIRLUKAST

Product NDC: 49884-304
Labeler Name: Par Pharmaceutical Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020547
Marketing Category: NDA
Start Marketing Date: 20101201

Package Information of ZAFIRLUKAST

Package NDC: 49884-304-02
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (49884-304-02)

NDC Information of ZAFIRLUKAST

NDC Code 49884-304-02
Proprietary Name ZAFIRLUKAST
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (49884-304-02)
Product NDC 49884-304
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Zafirlukast
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20101201
Marketing Category Name NDA
Labeler Name Par Pharmaceutical Inc.
Substance Name ZAFIRLUKAST
Strength Number 20
Strength Unit mg/1
Pharmaceutical Classes Leukotriene Receptor Antagonist [EPC],Leukotriene Receptor Antagonists [MoA]

Complete Information of ZAFIRLUKAST


General Information