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Montelukast - 0781-5560-13 - (Montelukast)

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Drug Information of Montelukast

Product NDC: 0781-5560
Proprietary Name: Montelukast
Non Proprietary Name: Montelukast
Active Ingredient(s): 10    mg/1 & nbsp;   Montelukast
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Montelukast

Product NDC: 0781-5560
Labeler Name: Sandoz Inc
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA200889
Marketing Category: ANDA
Start Marketing Date: 20120803

Package Information of Montelukast

Package NDC: 0781-5560-13
Package Description: 10 BLISTER PACK in 1 CARTON (0781-5560-13) > 10 TABLET, FILM COATED in 1 BLISTER PACK (0781-5560-06)

NDC Information of Montelukast

NDC Code 0781-5560-13
Proprietary Name Montelukast
Package Description 10 BLISTER PACK in 1 CARTON (0781-5560-13) > 10 TABLET, FILM COATED in 1 BLISTER PACK (0781-5560-06)
Product NDC 0781-5560
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Montelukast
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 20120803
Marketing Category Name ANDA
Labeler Name Sandoz 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


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