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Montelukast Sodium - 42291-623-30 - (Montelukast Sodium)

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Drug Information of Montelukast Sodium

Product NDC: 42291-623
Proprietary Name: Montelukast Sodium
Non Proprietary Name: Montelukast Sodium
Active Ingredient(s): 5    mg/1 & nbsp;   Montelukast Sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of Montelukast Sodium

Product NDC: 42291-623
Labeler Name: AvKARE, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200405
Marketing Category: ANDA
Start Marketing Date: 20130102

Package Information of Montelukast Sodium

Package NDC: 42291-623-30
Package Description: 30 TABLET, CHEWABLE in 1 BOTTLE (42291-623-30)

NDC Information of Montelukast Sodium

NDC Code 42291-623-30
Proprietary Name Montelukast Sodium
Package Description 30 TABLET, CHEWABLE in 1 BOTTLE (42291-623-30)
Product NDC 42291-623
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Montelukast Sodium
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20130102
Marketing Category Name ANDA
Labeler Name AvKARE, Inc.
Substance Name MONTELUKAST SODIUM
Strength Number 5
Strength Unit mg/1
Pharmaceutical Classes Leukotriene Receptor Antagonist [EPC],Leukotriene Receptor Antagonists [MoA]

Complete Information of Montelukast Sodium


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