NDC 50580-726

Zyrtec Allergy

Cetirizine Hydrochloride

Zyrtec Allergy is a Oral Tablet, Film Coated in the Human Otc Drug category. It is labeled and distributed by Johnson & Johnson Consumer Inc., Mcneil Consumer Healthcare Division. The primary component is Cetirizine Hydrochloride.

Product ID50580-726_8a189f49-dd6d-478a-aec7-6d2c888529b5
NDC50580-726
Product TypeHuman Otc Drug
Proprietary NameZyrtec Allergy
Generic NameCetirizine Hydrochloride
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2008-01-01
Marketing CategoryNDA / NDA
Application NumberNDA019835
Labeler NameJohnson & Johnson Consumer Inc., McNeil Consumer Healthcare Division
Substance NameCETIRIZINE HYDROCHLORIDE
Active Ingredient Strength10 mg/1
Pharm ClassesHistamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
NDC Exclude FlagN
Listing Certified Through2023-12-31

Packaging

NDC 50580-726-03

50 BLISTER PACK in 1 CARTON (50580-726-03) > 1 TABLET, FILM COATED in 1 BLISTER PACK
Marketing Start Date2008-01-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 50580-726-36 [50580072636]

Zyrtec Allergy TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA019835
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2008-01-01

NDC 50580-726-13 [50580072613]

Zyrtec Allergy TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA019835
Product TypeHUMAN OTC DRUG
Marketing Start Date2009-03-21

NDC 50580-726-03 [50580072603]

Zyrtec Allergy TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA019835
Product TypeHUMAN OTC DRUG
Marketing Start Date2008-01-01

NDC 50580-726-40 [50580072640]

Zyrtec Allergy TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA019835
Product TypeHUMAN OTC DRUG
Marketing Start Date2014-01-20

NDC 50580-726-93 [50580072693]

Zyrtec Allergy TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA019835
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2018-07-27

NDC 50580-726-92 [50580072692]

Zyrtec Allergy TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA019835
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-07-12

NDC 50580-726-51 [50580072651]

Zyrtec Allergy TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA019835
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2010-01-26

NDC 50580-726-32 [50580072632]

Zyrtec Allergy TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA019835
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2008-01-01

NDC 50580-726-38 [50580072638]

Zyrtec Allergy TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA019835
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2008-01-01

NDC 50580-726-90 [50580072690]

Zyrtec Allergy TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA019835
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-01-26

NDC 50580-726-91 [50580072691]

Zyrtec Allergy TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA019835
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-07-27

NDC 50580-726-66 [50580072666]

Zyrtec Allergy TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA019835
Product TypeHUMAN OTC DRUG
Marketing Start Date2008-01-01

NDC 50580-726-70 [50580072670]

Zyrtec Allergy TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA019835
Product TypeHUMAN OTC DRUG
Marketing Start Date2008-01-01

NDC 50580-726-30 [50580072630]

Zyrtec Allergy TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA019835
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2008-01-01

NDC 50580-726-50 [50580072650]

Zyrtec Allergy TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA019835
Product TypeHUMAN OTC DRUG
Marketing Start Date2010-01-26

NDC 50580-726-96 [50580072696]

Zyrtec Allergy TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA019835
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-05-30

NDC 50580-726-97 [50580072697]

Zyrtec Allergy TABLET, FILM COATED
Marketing CategoryNDA
Application NumberNDA019835
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-05-30

Drug Details

Active Ingredients

IngredientStrength
CETIRIZINE HYDROCHLORIDE10 mg/1

OpenFDA Data

SPL SET ID:b165db38-b302-4220-8627-77cb07bb078c
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1020026
  • 1014678
    • UPC Code
  • 0333337204361

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

    NDCBrand NameGeneric Name
    50580-726Zyrtec AllergyZyrtec Allergy
    50580-778Zyrtec AllergyZyrtec Allergy
    67751-192Zyrtec AllergyZyrtec Allergy
    50580-752Zyrtec AllergyZyrtec Allergy
    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
    0378-3635Cetirizine 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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