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Montelukast - 0781-5555-31 - (Montelukast)

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Drug Information of Montelukast

Product NDC: 0781-5555
Proprietary Name: Montelukast
Non Proprietary Name: Montelukast
Active Ingredient(s): 5    mg/1 & nbsp;   Montelukast
Administration Route(s): ORAL
Dosage Form(s): TABLET, CHEWABLE
Coding System: National Drug Codes(NDC)

Labeler Information of Montelukast

Product NDC: 0781-5555
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA091414
Marketing Category: ANDA
Start Marketing Date: 20120803

Package Information of Montelukast

Package NDC: 0781-5555-31
Package Description: 30 TABLET, CHEWABLE in 1 BOTTLE (0781-5555-31)

NDC Information of Montelukast

NDC Code 0781-5555-31
Proprietary Name Montelukast
Package Description 30 TABLET, CHEWABLE in 1 BOTTLE (0781-5555-31)
Product NDC 0781-5555
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Montelukast
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20120803
Marketing Category Name ANDA
Labeler Name Sandoz 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


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