escitalopram oxalate

Product NDC
33261-955
11-digit product format
332610955
Labeler code
33261
Product ID
33261-955_fff7cc6b-ece8-4ff9-942d-118822b5eae5
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
escitalopram oxalate
Dosage form
TABLET
Route
ORAL
Labeler
Aidarex Pharmaceuticals LLC
Application
ANDA090939
Marketing category
ANDA
Marketing start
2012-09-11
Marketing end
0000-00-00
Substance
ESCITALOPRAM OXALATE
Active strength
20 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 Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
04dce598-23c6-b7e7-c3dd-9b9cfd6e1615Product name620170718

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
33261-955-30escitalopram oxalate30 in 1 BOTTLE, PLASTICTABLET301
33261-955-90escitalopram oxalate90 in 1 BOTTLE, PLASTICTABLET901

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
33261-955ESCITALOPRAM OXALATE TABLET [AIDAREX PHARMACEUTICALS LLC]1Legacy NDC, 2 package rows20140107_dccbf03a-bab2-4307-a89f-70d2c3b762d2.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
351250escitalopram oxalate 20 MG Oral TabletPSNdccbf03a-bab2-4307-a89f-70d2c3b762d21
351250escitalopram 20 MG Oral TabletSCDdccbf03a-bab2-4307-a89f-70d2c3b762d21
351250escitalopram (as escitalopram oxalate) 20 MG Oral TabletSYdccbf03a-bab2-4307-a89f-70d2c3b762d21

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
33261-955-303326109553030 in 1 BOTTLE, PLASTICHistorical
33261-955-903326109559090 in 1 BOTTLE, PLASTICHistorical