SINGULAIR - 63629-1639-3 - (montelukast sodium)

Alphabetical Index


Drug Information of SINGULAIR

Product NDC: 63629-1639
Proprietary Name: SINGULAIR
Non Proprietary Name: montelukast sodium
Active Ingredient(s): 10    mg/1 & nbsp;   montelukast sodium
Administration Route(s): ORAL
Dosage Form(s): TABLET, FILM COATED
Coding System: National Drug Codes(NDC)

Labeler Information of SINGULAIR

Product NDC: 63629-1639
Labeler Name: Bryant Ranch Prepack
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020829
Marketing Category: NDA
Start Marketing Date: 19980220

Package Information of SINGULAIR

Package NDC: 63629-1639-3
Package Description: 60 TABLET, FILM COATED in 1 BOTTLE (63629-1639-3)

NDC Information of SINGULAIR

NDC Code 63629-1639-3
Proprietary Name SINGULAIR
Package Description 60 TABLET, FILM COATED in 1 BOTTLE (63629-1639-3)
Product NDC 63629-1639
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name montelukast sodium
Dosage Form Name TABLET, FILM COATED
Route Name ORAL
Start Marketing Date 19980220
Marketing Category Name NDA
Labeler Name Bryant Ranch Prepack
Substance Name MONTELUKAST SODIUM
Strength Number 10
Strength Unit mg/1
Pharmaceutical Classes Leukotriene Receptor Antagonist [EPC],Leukotriene Receptor Antagonists [MoA]

Complete Information of SINGULAIR


General Information