motion sickness

Product NDC
70677-0026
11-digit product format
706770026
Labeler code
70677
Product ID
70677-0026_431a15a8-3c2d-45a2-a966-431ef13becbf
Type
HUMAN OTC DRUG
Nonproprietary name
Meclizine HCl
Dosage form
TABLET
Route
ORAL
Labeler
Strategic Sourcing Services, LLC (Sunmark)
Application
part336
Marketing category
OTC MONOGRAPH FINAL
Marketing start
2002-06-24
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
70677-0026-1EA - Each70677-0026b72d50b2-4881-42c1-af66-7fea9591bbdb12017-06-15

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
70677-0026MOTION SICKNESS (MECLIZINE HCL) TABLET [STRATEGIC SOURCING SERVICES LLC]9Legacy NDC20250411_48c29625-7ca9-4bcd-8481-475b538b8bae.zip

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
70677-0026-1706770026011 BLISTER PACK in 1 CARTON (70677-0026-1) > 8 TABLET in 1 BLISTER PACK1 blister pack2002-06-240000-00-00NoNoCurrent