FDA.reportPublic FDA data

Escitalopram

Product NDC
51655-151
11-digit product format
516550151
Labeler code
51655
Product ID
51655-151_2ba31b0a-87b0-4949-871d-d682f12ba8cd
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Escitalopram
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Northwind Pharmaceuticals
Application
ANDA076765
Marketing category
ANDA
Marketing start
2014-03-21
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#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
51655-151-522026-01-08C16284748780-19d75b9d1-22da-f424-e053-dadaa90a57ce3986b4a9-0d51-4dce-935f-b9d3e097b380
51655-151-522020-01-31C16284748780-19d75b9d1-22da-f424-e053-dadaa90a57ce3986b4a9-0d51-4dce-935f-b9d3e097b380

DailyMed Socrata Ingredients#

Ingredient, Type, UNII table
IngredientTypeUNIIDailyMed labelSPL versionUploaded
ESCITALOPRAM OXALATEACTIVE INGREDIENT5U85DBW7LOESCITALOPRAM TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS]1
ESCITALOPRAMACTIVE MOIETY4O4S742ANYESCITALOPRAM TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS]1

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
51655-151ESCITALOPRAM TABLET, FILM COATED [NORTHWIND PHARMACEUTICALS]1Legacy NDC20140611_3986b4a9-0d51-4dce-935f-b9d3e097b380.zip