SINGULAIR - 55154-5028-0 - (montelukast sodium)

Alphabetical Index


Drug Information of SINGULAIR

Product NDC: 55154-5028
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: 55154-5028
Labeler Name: Cardinal Health
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA020829
Marketing Category: NDA
Start Marketing Date: 19980220

Package Information of SINGULAIR

Package NDC: 55154-5028-0
Package Description: 10 BLISTER PACK in 1 BAG (55154-5028-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK

NDC Information of SINGULAIR

NDC Code 55154-5028-0
Proprietary Name SINGULAIR
Package Description 10 BLISTER PACK in 1 BAG (55154-5028-0) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Product NDC 55154-5028
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 Cardinal Health
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