ESCITALOPRAM

Product NDC: 51655-021
11-digit product format: 516550021
Labeler code: 51655
Product ID: 51655-021_f3f7546d-0afc-46ba-8905-9e263ef1f293
Type: HUMAN PRESCRIPTION DRUG
Nonproprietary name: escitalopram oxalate
Dosage form: TABLET, FILM COATED
Route: ORAL
Labeler: Northwind Pharmaceuticals, LLC
Application: ANDA076765
Marketing category: ANDA
Marketing start: 2015-02-09
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: 2019-12-31
Current FDA listing: Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDC	Effective	Action	Document	Indexing SPL	Related label
51655-021-52	2026-01-08	C162847	48780-1	9d75b9d0-2d6d-f424-e053-dadaa90a57ce	0caa123d-3494-4443-afbe-5592f5c05b30
51655-021-52	2020-01-31	C162847	48780-1	9d75b9d0-2d6d-f424-e053-dadaa90a57ce	0caa123d-3494-4443-afbe-5592f5c05b30

Ingredient, Type, UNII table
Ingredient	Type	UNII	DailyMed label	SPL version	Uploaded
ESCITALOPRAM OXALATE	ACTIVE INGREDIENT	5U85DBW7LO	ESCITALOPRAM (ESCITALOPRAM OXALATE) TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS, LLC]	1
ESCITALOPRAM	ACTIVE MOIETY	4O4S742ANY	ESCITALOPRAM (ESCITALOPRAM OXALATE) TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS, LLC]	1

NDC, Dashboard title, SPL version table
NDC	Dashboard title	SPL version	Validation	Dashboard ZIP
51655-021	ESCITALOPRAM (ESCITALOPRAM OXALATE) TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS, LLC]	1	Legacy NDC	20150325_0caa123d-3494-4443-afbe-5592f5c05b30.zip