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Montelukast Sodium - 54868-6363-0 - (Montelukast Sodium)

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Drug Information of Montelukast Sodium

Product NDC: 54868-6363
Proprietary Name: Montelukast Sodium
Non Proprietary Name: Montelukast Sodium
Active Ingredient(s): 4    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: 54868-6363
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA078723
Marketing Category: ANDA
Start Marketing Date: 20120809

Package Information of Montelukast Sodium

Package NDC: 54868-6363-0
Package Description: 60 TABLET, CHEWABLE in 1 BOTTLE (54868-6363-0)

NDC Information of Montelukast Sodium

NDC Code 54868-6363-0
Proprietary Name Montelukast Sodium
Package Description 60 TABLET, CHEWABLE in 1 BOTTLE (54868-6363-0)
Product NDC 54868-6363
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Montelukast Sodium
Dosage Form Name TABLET, CHEWABLE
Route Name ORAL
Start Marketing Date 20120809
Marketing Category Name ANDA
Labeler Name Physicians Total Care, Inc.
Substance Name MONTELUKAST SODIUM
Strength Number 4
Strength Unit mg/1
Pharmaceutical Classes Leukotriene Receptor Antagonist [EPC],Leukotriene Receptor Antagonists [MoA]

Complete Information of Montelukast Sodium


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