Escitalopram

Product NDC
0143-9809
11-digit product format
001439809
Labeler code
0143
Product ID
0143-9809_322655e3-fff3-4292-abf5-fb9634227072
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Escitalopram
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
West-Ward Pharmaceuticals Corp
Application
ANDA078766
Marketing category
ANDA
Marketing start
2012-09-11
Marketing end
0000-00-00
Substance
ESCITALOPRAM OXALATE
Active strength
5 mg/1
Pharmacologic classes
Serotonin Reuptake Inhibitor [EPC],Serotonin Uptake Inhibitors [MoA]
NDC exclude flag
E
Listing certified through
2018-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0143-9809-01EA - Each0143-980972255429-3524-4bf7-b660-ac74081b473212013-03-03