NDC 37205-820

LEADER ALL DAY ALLERGY

Cetirizine

LEADER ALL DAY ALLERGY is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Cardinal Health. The primary component is Cetirizine Hydrochloride.

Product ID37205-820_c69e021b-e6d3-4e71-9208-0d981b58e724
NDC37205-820
Product TypeHuman Otc Drug
Proprietary NameLEADER ALL DAY ALLERGY
Generic NameCetirizine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2007-12-27
Marketing CategoryANDA / ANDA
Application NumberANDA077498
Labeler NameCardinal Health
Substance NameCETIRIZINE HYDROCHLORIDE
Active Ingredient Strength10 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 37205-820-75

90 TABLET in 1 BOTTLE (37205-820-75)
Marketing Start Date2007-12-27
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 37205-820-76 [37205082076]

LEADER ALL DAY ALLERGY TABLET
Marketing CategoryANDA
Application NumberANDA077498
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2007-12-27
Inactivation Date2020-01-31

NDC 37205-820-65 [37205082065]

LEADER ALL DAY ALLERGY TABLET
Marketing CategoryANDA
Application NumberANDA077498
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2007-12-27
Inactivation Date2020-01-31

NDC 37205-820-74 [37205082074]

LEADER ALL DAY ALLERGY TABLET
Marketing CategoryANDA
Application NumberANDA077498
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2007-12-27
Inactivation Date2020-01-31

NDC 37205-820-70 [37205082070]

LEADER ALL DAY ALLERGY TABLET
Marketing CategoryANDA
Application NumberANDA077498
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2007-12-27
Inactivation Date2020-01-31

NDC 37205-820-75 [37205082075]

LEADER ALL DAY ALLERGY TABLET
Marketing CategoryANDA
Application NumberANDA077498
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2007-12-27
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
CETIRIZINE HYDROCHLORIDE10 mg/1

OpenFDA Data

SPL SET ID:38e7396c-223a-4df6-9d39-fb4de5214269
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 1014678
    • UPC Code
  • 0096295123272
  • 0096295123067

    • Medicade Reported Pricing

    37205082076 ALL DAY ALLERGY 10 MG TABLET

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "LEADER ALL DAY ALLERGY" or generic name "Cetirizine"

    NDCBrand NameGeneric Name
    37205-820LEADER ALL DAY ALLERGYcetirizine
    70000-0380leader all day allergyCetirizine Hydrochloride
    51824-076CAREALL Cetirizine HClCetirizine
    0363-1040CetirizineCetirizine
    11673-219CetirizineCetirizine
    21695-878CetirizineCetirizine
    60505-4322CetirizineCetirizine
    60505-4668CetirizineCetirizine
    60505-4706CetirizineCetirizine
    67046-680CetirizineCetirizine
    37012-939Cetirizine HydrochlorideCetirizine
    65162-003Cetirizine HydrochlorideCetirizine
    65162-005Cetirizine HydrochlorideCetirizine
    65162-045Cetirizine HydrochlorideCetirizine
    65162-046Cetirizine HydrochlorideCetirizine
    65162-145Cetirizine HydrochlorideCetirizine
    65162-146Cetirizine HydrochlorideCetirizine
    65162-684Cetirizine HydrochlorideCetirizine
    71776-024ZerviateCetirizine
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