Home > National Drug Code (NDC) > Montelukast Sodium

Montelukast Sodium - 43063-380-15 - (Montelukast Sodium)

Alphabetical Index


Drug Information of Montelukast Sodium

Product NDC: 43063-380
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
Coding System: National Drug Codes(NDC)

Labeler Information of Montelukast Sodium

Product NDC: 43063-380
Labeler Name: PD-Rx Pharmaceuticals, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA090655
Marketing Category: ANDA
Start Marketing Date: 20120803

Package Information of Montelukast Sodium

Package NDC: 43063-380-15
Package Description: 15 TABLET in 1 BOTTLE, PLASTIC (43063-380-15)

NDC Information of Montelukast Sodium

NDC Code 43063-380-15
Proprietary Name Montelukast Sodium
Package Description 15 TABLET in 1 BOTTLE, PLASTIC (43063-380-15)
Product NDC 43063-380
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Montelukast Sodium
Dosage Form Name TABLET
Route Name ORAL
Start Marketing Date 20120803
Marketing Category Name ANDA
Labeler Name PD-Rx Pharmaceuticals, 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 Sodium


General Information