Eszopiclone

Product NDC
50090-5084
11-digit product format
500905084
Labeler code
50090
Product ID
50090-5084_dec7401c-9f85-4775-a971-1fbe53be91a2
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Eszopiclone
Dosage form
TABLET, COATED
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA091024
Marketing category
ANDA
Marketing start
2014-04-15
Marketing end
0000-00-00
Substance
ESZOPICLONE
Active strength
3 mg/1
DEA schedule
CIV
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
f65008ed-f925-2246-581a-e6a3201df7e4Product name520250107

FDA-Initiated Inactive NDC Indexing#

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50090-5084-0Eszopiclone30 in 1 BOTTLETABLET, COATED301

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50090-5084ESZOPICLONE TABLET, COATED [A-S MEDICATION SOLUTIONS]1Legacy NDC, 1 package rows20200804_44815d96-2157-454f-8dbb-d0b47f439d6b.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
485465eszopiclone 3 MG Oral TabletPSN44815d96-2157-454f-8dbb-d0b47f439d6b1
485465eszopiclone 3 MG Oral TabletSCD44815d96-2157-454f-8dbb-d0b47f439d6b1

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
50090-5084-05009050840030 TABLET, COATED in 1 BOTTLE (50090-5084-0) 2020-06-190000-00-00NoNoCurrent