MECLIZINE HYDROCHLORIDE

Product NDC
50090-4577
11-digit product format
500904577
Labeler code
50090
Product ID
50090-4577_7345346e-2e75-4217-88d8-5e23ff533496
Type
HUMAN PRESCRIPTION DRUG
Nonproprietary name
Meclizine Hydrocloride
Dosage form
TABLET
Route
ORAL
Labeler
A-S Medication Solutions
Application
ANDA040659
Marketing category
ANDA
Marketing start
2010-06-04
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
2022-12-31
Current FDA listing
Historical FDA.report record

FDA-Initiated Inactive NDC Indexing#

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
50090-4577-0EA - Each50090-4577a1338f97-f2e0-440a-aaf5-72d78d2366f612022-12-07
50090-4577-1EA - Each50090-4577dffbce0b-5481-4fd8-bd03-c7f5d5b8fd5a12021-08-05
50090-4577-4EA - Each50090-4577f7b89614-13ea-4691-a36f-6724e20c9d7712022-12-07
50090-4577-8EA - Each50090-457765335236-57f2-4073-b78b-498770dafe6b12022-12-07

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
50090-4577-05009045770020 TABLET in 1 BOTTLE (50090-4577-0) 20 tablet2019-10-040000-00-00NoNoCurrent
50090-4577-15009045770130 TABLET in 1 BOTTLE (50090-4577-1) 30 tablet2019-10-040000-00-00NoNoCurrent
50090-4577-45009045770410 TABLET in 1 BOTTLE (50090-4577-4) 10 tablet2019-10-040000-00-00NoNoCurrent
50090-4577-85009045770890 TABLET in 1 BOTTLE (50090-4577-8) 90 tablet2019-10-040000-00-00NoNoCurrent