Cetirizine Hydrochloride

Product NDC
30142-058
Type
HUMAN OTC DRUG
Nonproprietary name
Cetirizine Hydrochloride
Dosage form
TABLET, ORALLY DISINTEGRATING
Route
ORAL
Labeler
KROGER COMPANY
Application
ANDA213557
Marketing category
ANDA
Substance
CETIRIZINE HYDROCHLORIDE
Current FDA listing
Yes

Related Records

Packages

Package NDCDescriptionMarketing startMarketing endSampleStatus
30142-058-764 BLISTER PACK in 1 CARTON (30142-058-76) / 6 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK2021-03-08NoHistorical

Related DailyMed Labels

TitleManufacturerEffective dateTypeVersion
b8b2af96-af48-5f63-e053-2995a90a7d7cKROGER COMPANY | Aurohealth LLC | APL HEALTHCARE LIMITED2021-05-06Human OTC Drug Label3