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Montelukast Sodium - 55111-725-78 - (Montelukast Sodium)

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Drug Information of Montelukast Sodium

Product NDC: 55111-725
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, COATED
Coding System: National Drug Codes(NDC)

Labeler Information of Montelukast Sodium

Product NDC: 55111-725
Labeler Name: Dr.Reddy's Laboratories Limited
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA201582
Marketing Category: ANDA
Start Marketing Date: 20120806

Package Information of Montelukast Sodium

Package NDC: 55111-725-78
Package Description: 10 BLISTER PACK in 1 CARTON (55111-725-78) > 10 TABLET, COATED in 1 BLISTER PACK (55111-725-79)

NDC Information of Montelukast Sodium

NDC Code 55111-725-78
Proprietary Name Montelukast Sodium
Package Description 10 BLISTER PACK in 1 CARTON (55111-725-78) > 10 TABLET, COATED in 1 BLISTER PACK (55111-725-79)
Product NDC 55111-725
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Montelukast Sodium
Dosage Form Name TABLET, COATED
Route Name ORAL
Start Marketing Date 20120806
Marketing Category Name ANDA
Labeler Name Dr.Reddy's Laboratories Limited
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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