allergy relief

Product NDC
11822-0458
11-digit product format
118220458
Labeler code
11822
Product ID
11822-0458_33c3dfbb-6286-466f-9429-c8797788e1ac
Type
HUMAN OTC DRUG
Nonproprietary name
Cetirizine Hydrochloride
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
Rite Aid Corporation
Application
ANDA078336
Marketing category
ANDA
Marketing start
2008-01-16
Marketing end
0000-00-00
Substance
CETIRIZINE HYDROCHLORIDE
Active strength
10 mg/1
NDC exclude flag
No
Listing certified through
2021-12-31
Current FDA listing
Historical FDA.report record

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
11822-0458-11182204580114 BLISTER PACK in 1 CARTON (11822-0458-1) > 1 TABLET, FILM COATED in 1 BLISTER PACK14 blister pack2008-01-160000-00-00NoNoCurrent
11822-0458-2118220458021 BOTTLE in 1 CARTON (11822-0458-2) > 30 TABLET, FILM COATED in 1 BOTTLE1 bottle2008-01-160000-00-00NoNoCurrent
11822-0458-3118220458031 BOTTLE in 1 CARTON (11822-0458-3) > 60 TABLET, FILM COATED in 1 BOTTLE1 bottle2008-01-160000-00-00NoNoCurrent
11822-0458-4118220458041 BOTTLE in 1 CARTON (11822-0458-4) > 120 TABLET, FILM COATED in 1 BOTTLE1 bottle2008-01-160000-00-00NoNoCurrent
11822-0458-6118220458061 BOTTLE in 1 CARTON (11822-0458-6) > 45 TABLET, FILM COATED in 1 BOTTLE1 bottle2008-01-160000-00-00NoNoCurrent
11822-0458-7118220458071 BOTTLE in 1 CARTON (11822-0458-7) > 300 TABLET, FILM COATED in 1 BOTTLE1 bottle2020-05-180000-00-00NoNoCurrent
11822-0458-8118220458081 BOTTLE in 1 CARTON (11822-0458-8) > 90 TABLET, FILM COATED in 1 BOTTLE1 bottle2020-05-180000-00-00NoNoCurrent