Hives Relief

Product NDC
0363-6340
11-digit product format
003636340
Labeler code
0363
Product ID
0363-6340_4d2c69cb-1f56-68a5-e063-6394a90a7074
Type
HUMAN OTC DRUG
Nonproprietary name
Cetirizine Tablets
Dosage form
TABLET, FILM COATED
Route
ORAL
Labeler
WALGREEN COMPANY
Application
ANDA078862
Marketing category
ANDA
Marketing start
2026-03-20
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
2027-12-31
Current FDA listing
Yes

Additional Listing Data#

Finished product
Yes
Brand name base
Hives Relief
Listing expiration
2027-12-31

Active Ingredients#

Ingredient, Strength table
IngredientStrength
CETIRIZINE HYDROCHLORIDE10 mg/1

Harmonized Identifiers#

Field, Values table
FieldValues
Unii64O047KTOA
Rxcui1014678

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
c505bb17-4ff9-45f9-ac2d-bb9c8c9d35beProduct name120200304
a255659f-db40-429d-8c07-5f173f330d9cProduct name120190402

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
0363-6340-13Hives Relief30 in 1 BOTTLE, PLASTICTABLET, FILM COATED302

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYDailyMedSPL version
1014678cetirizine HCl 10 MG Oral TabletPSN4526b65c-b0e7-180c-e063-6394a90ae9162
1014678cetirizine hydrochloride 10 MG Oral TabletSCD4526b65c-b0e7-180c-e063-6394a90ae9162
1014678cetirizine HCl 10 MG Oral TabletSY4526b65c-b0e7-180c-e063-6394a90ae9162

Packages#

Package NDC, 11-digit format, Description table
Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
0363-6340-130036363401330 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0363-6340-13) 2026-03-20NoNoCurrent