ESZOPICLONE

Product NDC
71335-0148
11-digit product format
713350148
Labeler code
71335
Product ID
71335-0148_ececb1a7-5aa7-4e5e-bb90-c491c55e7523
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
ESZOPICLONE
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
ANDA091113
Marketing category
ANDA
Marketing start
2014-09-25
Marketing end
0000-00-00
Substance
ESZOPICLONE
Active strength
2 mg/1
DEA schedule
CIV
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

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

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71335-0148-1ESZOPICLONE30 in 1 BOTTLETABLET, FILM COATED30102
71335-0148-2ESZOPICLONE60 in 1 BOTTLETABLET, FILM COATED60102
71335-0148-3ESZOPICLONE90 in 1 BOTTLETABLET, FILM COATED90102
71335-0148-4ESZOPICLONE120 in 1 BOTTLETABLET, FILM COATED120102
71335-0148-5ESZOPICLONE20 in 1 BOTTLETABLET, FILM COATED20102
71335-0148-6ESZOPICLONE100 in 1 BOTTLETABLET, FILM COATED100102
71335-0148-7ESZOPICLONE28 in 1 BOTTLETABLET, FILM COATED28102
71335-0148-8ESZOPICLONE10 in 1 BOTTLETABLET, FILM COATED10102

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71335-0148-8EA - Each71335-014867967b93-a2d2-46f5-981f-b5aa593f884f12022-08-04

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71335-0148ESZOPICLONE TABLET, FILM COATED [BRYANT RANCH PREPACK]102Legacy NDC, 8 package rows20240524_a09a2e9c-dc23-43df-831f-e6c63547d350.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
485442eszopiclone 2 MG Oral TabletPSNa09a2e9c-dc23-43df-831f-e6c63547d350102
485442eszopiclone 2 MG Oral TabletSCDa09a2e9c-dc23-43df-831f-e6c63547d350102

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
71335-0148-17133501480130 TABLET, FILM COATED in 1 BOTTLE (71335-0148-1) 2017-01-030000-00-00NoNoCurrent
71335-0148-27133501480260 TABLET, FILM COATED in 1 BOTTLE (71335-0148-2) 2017-01-030000-00-00NoNoCurrent
71335-0148-37133501480390 TABLET, FILM COATED in 1 BOTTLE (71335-0148-3) 2017-01-030000-00-00NoNoCurrent
71335-0148-471335014804120 TABLET, FILM COATED in 1 BOTTLE (71335-0148-4) 2017-01-030000-00-00NoNoCurrent
71335-0148-57133501480520 TABLET, FILM COATED in 1 BOTTLE (71335-0148-5) 2017-01-030000-00-00NoNoCurrent
71335-0148-671335014806100 TABLET, FILM COATED in 1 BOTTLE (71335-0148-6) 2017-01-030000-00-00NoNoCurrent
71335-0148-77133501480728 TABLET, FILM COATED in 1 BOTTLE (71335-0148-7) 2017-01-030000-00-00NoNoCurrent
71335-0148-87133501480810 TABLET, FILM COATED in 1 BOTTLE (71335-0148-8) 2017-01-030000-00-00NoNoCurrent