Allergy Relief

Product NDC
55910-930
11-digit product format
559100930
Labeler code
55910
Product ID
55910-930_7fae39be-7b63-443c-a917-2df562135a84
Type
HUMAN OTC DRUG
Nonproprietary name
Cetirizine HCl
Dosage form
TABLET
Route
ORAL
Labeler
Dolgencorp, Inc. (DOLLAR GENERAL & REXALL)
Application
ANDA209274
Marketing category
ANDA
Marketing start
2023-02-28
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
2026-12-31
Current FDA listing
Yes

Related Records

Related UNII Ingredients

UNIIPreferred termRegistry numberMatched term
64O047KTOACETIRIZINE HYDROCHLORIDE83881-52-1CETIRIZINE HYDROCHLORIDE

Packages

Package NDC11-digit formatDescriptionMarketing startSampleExclude flagStatus
55910-930-45559100930451 BOTTLE, PLASTIC in 1 BOX (55910-930-45) / 45 TABLET in 1 BOTTLE, PLASTIC2023-02-28NoNoHistorical
55910-930-90559100930901 BOTTLE, PLASTIC in 1 BOX (55910-930-90) / 90 TABLET in 1 BOTTLE, PLASTIC2023-02-28NoNoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
Drug FactsDolgencorp, Inc. (DOLLAR GENERAL & REXALL)2023-09-14HUMAN OTC DRUG LABEL5