"70357-002-30" National Drug Code (NDC)

NDC Code	70357-002-30
Package Description	30 TABLET, FILM COATED in 1 BOTTLE (70357-002-30)
Product NDC	70357-002
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Montelukast
Non-Proprietary Name	Montelukast
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20141201
Marketing Category Name	ANDA
Application Number	ANDA202859
Manufacturer	ASE Direct, Inc.
Substance Name	MONTELUKAST SODIUM
Strength	10
Strength Unit	mg/1
Pharmacy Classes	Leukotriene Receptor Antagonist [EPC],Leukotriene Receptor Antagonists [MoA]