Meclizine Hydrochloride

Product NDC
42291-609
11-digit product format
422910609
Labeler code
42291
Product ID
42291-609_e7b647dc-d59f-4e05-e053-2995a90a4418
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Meclizine Hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
AvKARE
Application
ANDA201451
Marketing category
ANDA
Marketing start
2012-05-11
Marketing end
0000-00-00
Substance
MECLIZINE HYDROCHLORIDE
Active strength
25 mg/1
Pharmacologic classes
Antiemetic [EPC], Emesis Suppression [PE]
NDC exclude flag
No
Listing certified through
2023-12-31
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
42291-609-10EA - Each42291-6092fed8567-e6da-4b1c-96b7-d04e9bb4934f12013-02-13
42291-609-90EA - Each42291-6098280dcf3-e2ab-4d85-8b21-4484387021c012013-02-13

DailyMed Socrata Ingredients#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
42291-609MECLIZINE HYDROCHLORIDE TABLET [AVKARE]12Legacy NDC20230621_413746b7-71a4-5d34-d0fe-88fa9ecd119d.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
42291-609-10422910609101000 TABLET in 1 BOTTLE (42291-609-10) 1000 tablet2012-05-110000-00-00NoNoCurrent
42291-609-904229106099090 TABLET in 1 BOTTLE (42291-609-90) 90 tablet2012-05-110000-00-00NoNoCurrent