24 Hour Allergy

Product NDC
66715-6850
11-digit product format
667156850
Labeler code
66715
Product ID
66715-6850_f97197db-b659-4f80-be45-6062493c5c65
Type
HUMAN OTC DRUG
Nonproprietary name
Cetirizine hydrochloride
Dosage form
TABLET
Route
ORAL
Labeler
Lil' Drug Store Products, Inc
Application
ANDA078780
Marketing category
ANDA
Marketing start
2014-11-01
Marketing end
2023-01-17
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

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionUnitsMarketing startMarketing endSampleExclude flagStatus
66715-6850-0667156850001 BLISTER PACK in 1 CARTON (66715-6850-0) > 5 TABLET in 1 BLISTER PACK1 blister pack2014-11-012023-01-17NoNoCurrent