Meclizine Hydrochloride

Product NDC
71335-1872
11-digit product format
713351872
Labeler code
71335
Product ID
71335-1872_34f55f1a-8892-49e5-a2dd-38b59bb68bd4
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Meclizine Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Bryant Ranch Prepack
Application
NDA010721
Marketing category
NDA AUTHORIZED GENERIC
Marketing start
2020-01-15
Substance
MECLIZINE HYDROCHLORIDE
Active strength
12.5 mg/1
Pharmacologic classes
Antiemetic [EPC], Emesis Suppression [PE]
NDC exclude flag
No
Listing certified through
2026-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Meclizine Hydrochloride
Listing expiration
2026-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
MECLIZINE HYDROCHLORIDE12.5 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
UniiHDP7W44CIO
Rxcui995624

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ac6963c4-31c6-325f-ee58-83a0a06597adProduct name520221206
7792dadb-52b6-46b6-8fdf-80b1171065b5Product name120180810

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71335-1872-1Meclizine Hydrochloride30 in 1 BOTTLETABLET30103
71335-1872-2Meclizine Hydrochloride60 in 1 BOTTLETABLET60103
71335-1872-3Meclizine Hydrochloride90 in 1 BOTTLETABLET90103
71335-1872-4Meclizine Hydrochloride28 in 1 BOTTLETABLET28103
71335-1872-5Meclizine Hydrochloride20 in 1 BOTTLETABLET20103
71335-1872-6Meclizine Hydrochloride120 in 1 BOTTLETABLET120103
71335-1872-7Meclizine Hydrochloride100 in 1 BOTTLETABLET100103
71335-1872-8Meclizine Hydrochloride10 in 1 BOTTLETABLET10103

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
71335-1872-1EA - Each71335-18728808e9d0-afda-4ae2-a293-dc42598607c112026-01-08
71335-1872-3EA - Each71335-1872f48ef210-b9bb-4b6a-aaaf-9e34ff40a33e12026-01-08
71335-1872-5EA - Each71335-1872c8bee1f1-6bcd-4e25-afd5-311e172eea4812026-01-08

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71335-1872MECLIZINE HYDROCHLORIDE TABLET [BRYANT RANCH PREPACK]102Current NDC, Legacy NDC, 8 package rows20230607_112103bc-25e2-42cf-8542-ba1d3392a2c3.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
995624meclizine HCl 12.5 MG Oral TabletPSN112103bc-25e2-42cf-8542-ba1d3392a2c3103
995624meclizine hydrochloride 12.5 MG Oral TabletSCD112103bc-25e2-42cf-8542-ba1d3392a2c3103

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
71335-1872-17133518720130 TABLET in 1 BOTTLE (71335-1872-1) 30 tablet2021-06-280000-00-00NoNoCurrent
71335-1872-27133518720260 TABLET in 1 BOTTLE (71335-1872-2) 60 tablet2021-06-280000-00-00NoNoCurrent
71335-1872-37133518720390 TABLET in 1 BOTTLE (71335-1872-3) 90 tablet2021-06-280000-00-00NoNoCurrent
71335-1872-47133518720428 TABLET in 1 BOTTLE (71335-1872-4) 28 tablet2021-06-280000-00-00NoNoCurrent
71335-1872-57133518720520 TABLET in 1 BOTTLE (71335-1872-5) 20 tablet2021-06-280000-00-00NoNoCurrent
71335-1872-671335187206120 TABLET in 1 BOTTLE (71335-1872-6) 120 tablet2021-06-280000-00-00NoNoCurrent
71335-1872-771335187207100 TABLET in 1 BOTTLE (71335-1872-7) 100 tablet2021-06-280000-00-00NoNoCurrent
71335-1872-87133518720810 TABLET in 1 BOTTLE (71335-1872-8) 10 tablet2021-06-28NoNoHistorical