Allergy Relief

Product NDC
37012-458
11-digit product format
370120458
Labeler code
37012
Product ID
37012-458_4e9663c5-7e14-4d3c-944a-fbcb4b1142f2
Type
HUMAN OTC DRUG
Nonproprietary name
Cetirizine Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Shopko Stores Operating Co., LLC
Application
ANDA078336
Marketing category
ANDA
Marketing start
2013-07-08
Marketing end
0000-00-00
Substance
CETIRIZINE HYDROCHLORIDE
Active strength
10 mg/1
NDC exclude flag
No
Listing certified through
2020-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
37012-458-06370120458061 BOTTLE in 1 CARTON (37012-458-06) > 70 TABLET, FILM COATED in 1 BOTTLE1 bottle2014-06-270000-00-00NoNoCurrent
37012-458-39370120458391 BOTTLE in 1 CARTON (37012-458-39) > 30 TABLET, FILM COATED in 1 BOTTLE1 bottle2013-10-170000-00-00NoNoCurrent
37012-458-663701204586614 BLISTER PACK in 1 CARTON (37012-458-66) > 1 TABLET, FILM COATED in 1 BLISTER PACK14 blister pack2013-09-090000-00-00NoNoCurrent
37012-458-72370120458721 BOTTLE in 1 CARTON (37012-458-72) > 60 TABLET, FILM COATED in 1 BOTTLE1 bottle2013-07-080000-00-00NoNoCurrent
37012-458-95370120458951 BOTTLE in 1 CARTON (37012-458-95) > 45 TABLET, FILM COATED in 1 BOTTLE1 bottle2016-12-050000-00-00NoNoCurrent