escitalopram

Product NDC
54879-010
11-digit product format
548790010
Labeler code
54879
Product ID
54879-010_b33ea9f7-1fa9-4ba8-8a3c-6f9897015044
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
escitalopram
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
STI Pharma LLC
Application
ANDA077512
Marketing category
ANDA
Marketing start
2013-09-12
Marketing end
0000-00-00
Substance
ESCITALOPRAM OXALATE
Active strength
10 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
54879-010-01EA - Each54879-0105f498315-b178-46fa-a8d0-b7ae209d020012014-09-03