Escitalopram

Product NDC: 63629-8241
11-digit product format: 636298241
Labeler code: 63629
Product ID: 63629-8241_8737d702-0af8-4f2d-a457-e4888eed5de5
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: Escitalopram
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: Bryant Ranch Prepack
Application: ANDA078032
Marketing category: ANDA
Marketing start: 2012-03-15
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: No
Listing certified through: 2020-12-31
Current FDA listing: Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product concept	Relation	Version	Effective
04dce598-23c6-b7e7-c3dd-9b9cfd6e1615	Product name	6	20170718

UNII, Preferred term, Registry number table
UNII	Preferred term	Registry number	Matched term
5U85DBW7LO	ESCITALOPRAM OXALATE	219861-08-2	ESCITALOPRAM OXALATE
4O4S742ANY	ESCITALOPRAM	128196-01-0	Escitalopram

RxCUI, RxNorm string, TTY table
RxCUI	RxNorm string	TTY	DailyMed	SPL version
349332	escitalopram oxalate 10 MG Oral Tablet	PSN	d96efcdf-88ac-4153-9a38-4cd47e5bbb5b	9
349332	escitalopram 10 MG Oral Tablet	SCD	d96efcdf-88ac-4153-9a38-4cd47e5bbb5b	9
349332	escitalopram (as escitalopram oxalate) 10 MG Oral Tablet	SY	d96efcdf-88ac-4153-9a38-4cd47e5bbb5b	9

Package NDC, 11-digit format, Description table
Package NDC	11-digit format	Description	Marketing start	Marketing end	Sample	Exclude flag	Status
63629-8241-1	63629824101	30 TABLET, FILM COATED in 1 BOTTLE (63629-8241-1)	2019-09-17	0000-00-00	No	No	Current