"57237-093-90" National Drug Code (NDC)

NDC Code	57237-093-90
Package Description	90 TABLET, FILM COATED in 1 BOTTLE (57237-093-90)
Product NDC	57237-093
Product Type Name	HUMAN PRESCRIPTION DRUG
Proprietary Name	Escitalopram
Non-Proprietary Name	Escitalopram Oxalate
Dosage Form	TABLET, FILM COATED
Usage	ORAL
Start Marketing Date	20120911
Marketing Category Name	ANDA
Application Number	ANDA090432
Manufacturer	Citron Pharma LLC
Substance Name	ESCITALOPRAM OXALATE
Strength	10
Strength Unit	mg/1
Pharmacy Classes	Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]