Cetirizine

Product NDC
0363-1040
11-digit product format
003631040
Labeler code
0363
Product ID
0363-1040_17d5aaef-5e83-cdfa-8ce3-4c7d4496ba22
Type
HUMAN OTC DRUG
Nonproprietary name
Cetirizine
Dosage form
CAPSULE, LIQUID FILLED
Route
ORAL
Labeler
Walgreens
Application
ANDA207235
Marketing category
ANDA
Marketing start
2017-07-03
Marketing end
2023-05-31
Substance
CETIRIZINE HYDROCHLORIDE
Active strength
10 mg/1
NDC exclude flag
No
Listing certified through
0000-00-00
Current FDA listing
Historical FDA.report record

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
0363-1040-02EA - Each0363-1040512e446c-8cac-40d2-baaa-e8051c273f7712022-06-06

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
0363-1040-02003631040021 BOTTLE in 1 CARTON (0363-1040-02) > 25 CAPSULE, LIQUID FILLED in 1 BOTTLE1 bottle2017-07-032023-01-31NoNoCurrent
0363-1040-04003631040041 BOTTLE in 1 BLISTER PACK (0363-1040-04) > 40 CAPSULE, LIQUID FILLED in 1 BOTTLE1 bottle2017-07-032023-05-31NoNoCurrent