Allergy Relief

Product NDC
69230-303
11-digit product format
692300303
Labeler code
69230
Product ID
69230-303_f14403cd-2f62-4c7b-903a-ec8e55f40fa9
Type
HUMAN OTC DRUG
Nonproprietary name
Cetirizine HCl
Dosage form
CAPSULE
Route
ORAL
Labeler
Camber Consumer Care
Application
ANDA207235
Marketing category
ANDA
Marketing start
2018-12-31
Marketing end
0000-00-00
Substance
CETIRIZINE HYDROCHLORIDE
Active strength
10 mg/1
Pharmacologic classes
Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
NDC exclude flag
No
Listing certified through
2023-12-31
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
69230-303-24EA - Each69230-303ef2e07c3-bb40-4c80-b6f1-79c448b4c2af12019-03-12
69230-303-40EA - Each69230-303a2fe3a7f-9643-44d6-bf73-5f3cabacbfeb12019-03-12

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startMarketing endSampleExclude flagStatus
69230-303-24692300303241 BOTTLE, PLASTIC in 1 BOX (69230-303-24) > 25 CAPSULE in 1 BOTTLE, PLASTIC2018-12-310000-00-00NoNoCurrent
69230-303-40692300303401 BOTTLE, PLASTIC in 1 BOX (69230-303-40) > 40 CAPSULE in 1 BOTTLE, PLASTIC2018-12-310000-00-00NoNoCurrent