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Montelukast Sodium - 42291-621-90 - (Montelukast Sodium)

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Drug Information of Montelukast Sodium

Product NDC: 42291-621
Proprietary Name: Montelukast Sodium
Non Proprietary Name: Montelukast Sodium
Active Ingredient(s): 10    mg/1 & nbsp;   Montelukast Sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Montelukast Sodium

Product NDC: 42291-621
Labeler Name: AvKARE, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201522
Marketing Category: ANDA
Start Marketing Date: 20120810

Package Information of Montelukast Sodium

Package NDC: 42291-621-90
Package Description: 90 TABLET, FILM COATED in 1 BOTTLE (42291-621-90)

NDC Information of Montelukast Sodium

NDC Code 42291-621-90
Proprietary Name Montelukast Sodium
Package Description 90 TABLET, FILM COATED in 1 BOTTLE (42291-621-90)
Product NDC 42291-621
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Montelukast Sodium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120810
Marketing Category Name ANDA
Labeler Name AvKARE, Inc.
Substance Name MONTELUKAST SODIUM
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Leukotriene Receptor Antagonist [EPC],Leukotriene Receptor Antagonists [MoA]

Complete Information of Montelukast Sodium


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