MECLIZINE HYDROCHLORIDE

Product NDC
10544-081
11-digit product format
105440081
Labeler code
10544
Product ID
10544-081_1169212a-8191-5337-e054-00144ff88e88
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Meclizine Hydrocloride
Dosage form
TABLET
Route
ORAL
Labeler
Blenheim Pharmacal, Inc.
Application
ANDA040659
Marketing category
ANDA
Marketing start
2012-08-01
Marketing end
0000-00-00
Substance
MECLIZINE HYDROCHLORIDE
Active strength
25 mg/1
Pharmacologic classes
Antiemetic [EPC],Emesis Suppression [PE]
NDC exclude flag
E
Listing certified through
2017-12-31
Current FDA listing
Historical FDA.report record

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ac6963c4-31c6-325f-ee58-83a0a06597adProduct name520221206

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
10544-081-302020-01-31C16284748780-19d75b9d0-7447-f424-e053-dadaa90a57ceMECLIZINE HYDROCHLORIDE TABLETS, USP Rx only

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
10544-081-30MECLIZINE HYDROCHLORIDE30 in 1 BOTTLETABLET302

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
10544-081MECLIZINE HYDROCHLORIDE (MECLIZINE HYDROCLORIDE) TABLET [BLENHEIM PHARMACAL, INC.]2Legacy NDC, 1 package rows20150316_1167fc42-ed45-2c39-e054-00144ff88e88.zip

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
995666meclizine HCl 25 MG Oral TabletPSN1167fc42-ed45-2c39-e054-00144ff88e882
995666meclizine hydrochloride 25 MG Oral TabletSCD1167fc42-ed45-2c39-e054-00144ff88e882

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionStatus
10544-081-301054400813030 in 1 BOTTLEHistorical