NDC 63629-3708

Cetirizine

Cetirizine Hydrochloride

Cetirizine is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is Cetirizine Hydrochloride.

Product ID63629-3708_9c17ec04-0a0d-4ce9-a70f-9730ffd49ec8
NDC63629-3708
Product TypeHuman Otc Drug
Proprietary NameCetirizine
Generic NameCetirizine Hydrochloride
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2008-01-16
Marketing CategoryANDA / ANDA
Application NumberANDA078336
Labeler NameBryant Ranch Prepack
Substance NameCETIRIZINE HYDROCHLORIDE
Active Ingredient Strength10 mg/1
NDC Exclude FlagE
Listing Certified Through2017-12-31

Packaging

NDC 63629-3708-8

60 TABLET in 1 BOTTLE (63629-3708-8)
Marketing Start Date2008-01-16
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 63629-3708-5 [63629370805]

Cetirizine TABLET
Marketing CategoryANDA
Application NumberANDA078336
Product TypeHUMAN OTC DRUG
Marketing Start Date2008-01-16
Inactivation Date2019-11-27

NDC 63629-3708-1 [63629370801]

Cetirizine TABLET
Marketing CategoryANDA
Application NumberANDA078336
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2008-01-16
Inactivation Date2019-11-27

NDC 63629-3708-8 [63629370808]

Cetirizine TABLET
Marketing CategoryANDA
Application NumberANDA078336
Product TypeHUMAN OTC DRUG
Marketing Start Date2008-01-16
Inactivation Date2019-11-27

NDC 63629-3708-7 [63629370807]

Cetirizine TABLET
Marketing CategoryANDA
Application NumberANDA078336
Product TypeHUMAN OTC DRUG
Marketing Start Date2008-01-16
Inactivation Date2019-11-27

NDC 63629-3708-3 [63629370803]

Cetirizine TABLET
Marketing CategoryANDA
Application NumberANDA078336
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2008-01-16
Inactivation Date2019-11-27

NDC 63629-3708-2 [63629370802]

Cetirizine TABLET
Marketing CategoryANDA
Application NumberANDA078336
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2008-01-16
Inactivation Date2019-11-27

NDC 63629-3708-6 [63629370806]

Cetirizine TABLET
Marketing CategoryANDA
Application NumberANDA078336
Product TypeHUMAN OTC DRUG
Marketing Start Date2008-01-16
Inactivation Date2019-11-27

NDC 63629-3708-9 [63629370809]

Cetirizine TABLET
Marketing CategoryANDA
Application NumberANDA078336
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-07-24
Inactivation Date2019-11-27

NDC 63629-3708-4 [63629370804]

Cetirizine TABLET
Marketing CategoryANDA
Application NumberANDA078336
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2008-01-16
Inactivation Date2019-11-27

Drug Details

Active Ingredients

IngredientStrength
CETIRIZINE HYDROCHLORIDE10 mg/1

OpenFDA Data

SPL SET ID:6e7cc082-fa81-40cc-a1a6-41fd4f6a8c04
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1014678

    • NDC Crossover Matching brand name "Cetirizine" or generic name "Cetirizine Hydrochloride"

    NDCBrand NameGeneric Name
    0363-1040CetirizineCetirizine
    70518-1705CetirizineCetirizine
    70518-1652CetirizineCetirizine
    71610-123CetirizineCetirizine
    0615-7522CetirizineCetirizine
    75921-402CetirizineCetirizine
    0904-6717CetirizineCetirizine
    11673-219CetirizineCetirizine
    21695-878CetirizineCetirizine
    60505-4668CetirizineCetirizine
    60505-4322CetirizineCetirizine
    63629-3708CetirizineCetirizine
    67046-680CetirizineCetirizine
    55154-8081CetirizineCetirizine
    60505-4706CetirizineCetirizine
    70518-2335CetirizineCetirizine
    0363-4101allergy reliefCetirizine Hydrochloride
    0113-7002Basic Care All Day AllergyCetirizine Hydrochloride
    0113-7036BASIC CARE ALL DAY ALLERGYCetirizine hydrochloride
    0121-4780Cetirizine HydrochlorideCetirizine Hydrochloride
    0179-8301Cetirizine HydrochlorideCetirizine Hydrochloride
    0179-8302Cetirizine HydrochlorideCetirizine Hydrochloride
    0363-0471Cetirizine HydrochlorideCetirizine Hydrochloride
    0363-9899Cetirizine HydrochlorideCetirizine Hydrochloride
    0363-0068Cetirizine Hydrochloride (Allergy)Cetirizine Hydrochloride
    0363-9602Cetirizine Hydrochloride (Allergy)Cetirizine Hydrochloride
    0363-3311childrens allergy reliefCetirizine Hydrochloride
    0363-3393childrens allergy reliefCetirizine Hydrochloride
    0363-4025Childrens Cetirizine HydrochlorideCetirizine Hydrochloride
    0363-1884childrens dye free wal zyrcetirizine Hydrochloride
    0363-0595Childrens Wal Zyr 24 Hour Allergycetirizine Hydrochloride
    0363-0974Childrens Wal Zyr Allergycetirizine hydrochloride
    0363-1974dye free wal zyrcetirizine hydrochloride
    0113-0981Good Sense All Day Allergycetirizine hydrochloride
    0113-1036good sense all day allergyCetirizine hydrochloride
    0113-9458Good Sense all day allergyCetirizine Hydrochloride
    0363-0276wal zyrCetirizine Hydrochloride
    0363-0495Wal ZyrCetirizine Hydrochloride
    0363-2088Wal-ZyrCetirizine Hydrochloride
    0363-2102Wal-ZyrCetirizine Hydrochloride
    0363-2106Wal-ZyrCetirizine Hydrochloride
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