NDC 11523-7200

Claritin Liqui-Gels

Loratadine

Claritin Liqui-Gels is a Oral Capsule, Liquid Filled in the Human Otc Drug category. It is labeled and distributed by Bayer Healthcare Llc.. The primary component is Loratadine.

Product ID11523-7200_7093af92-b669-3183-e053-2a91aa0a69ac
NDC11523-7200
Product TypeHuman Otc Drug
Proprietary NameClaritin Liqui-Gels
Generic NameLoratadine
Dosage FormCapsule, Liquid Filled
Route of AdministrationORAL
Marketing Start Date2008-06-16
Marketing CategoryNDA / NDA
Application NumberNDA021952
Labeler NameBayer HealthCare LLC.
Substance NameLORATADINE
Active Ingredient Strength10 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 11523-7200-1

1 BLISTER PACK in 1 CARTON (11523-7200-1) > 10 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
Marketing Start Date2008-06-16
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 11523-7200-1 [11523720001]

Claritin Liqui-Gels CAPSULE, LIQUID FILLED
Marketing CategoryNDA
Application NumberNDA021952
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2008-06-16

NDC 11523-7200-5 [11523720005]

Claritin Liqui-Gels CAPSULE, LIQUID FILLED
Marketing CategoryNDA
Application NumberNDA021952
Product TypeHUMAN OTC DRUG
Marketing Start Date2008-06-16
Marketing End Date2016-01-01

NDC 11523-7200-4 [11523720004]

Claritin Liqui-Gels CAPSULE, LIQUID FILLED
Marketing CategoryNDA
Application NumberNDA021952
Product TypeHUMAN OTC DRUG
Marketing Start Date2008-06-16
Marketing End Date2016-01-01

NDC 11523-7200-3 [11523720003]

Claritin Liqui-Gels CAPSULE, LIQUID FILLED
Marketing CategoryNDA
Application NumberNDA021952
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2008-06-16
Marketing End Date2016-01-01

NDC 11523-7200-8 [11523720008]

Claritin Liqui-Gels CAPSULE, LIQUID FILLED
Marketing CategoryNDA
Application NumberNDA021952
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2008-06-16

NDC 11523-7200-9 [11523720009]

Claritin Liqui-Gels CAPSULE, LIQUID FILLED
Marketing CategoryNDA
Application NumberNDA021952
Product TypeHUMAN OTC DRUG
Marketing Start Date2008-06-16

NDC 11523-7200-7 [11523720007]

Claritin Liqui-Gels CAPSULE, LIQUID FILLED
Marketing CategoryNDA
Application NumberNDA021952
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2008-06-16
Marketing End Date2016-01-01

NDC 11523-7200-6 [11523720006]

Claritin Liqui-Gels CAPSULE, LIQUID FILLED
Marketing CategoryNDA
Application NumberNDA021952
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2008-06-16

NDC 11523-7200-2 [11523720002]

Claritin Liqui-Gels CAPSULE, LIQUID FILLED
Marketing CategoryNDA
Application NumberNDA021952
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2008-06-16
Marketing End Date2016-01-01

Drug Details

Active Ingredients

IngredientStrength
LORATADINE10 mg/1

OpenFDA Data

SPL SET ID:8e14b61f-faf6-43a8-a080-75f64514217a
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 828269
  • 836338
    • UPC Code
  • 0041100806109

    • Medicade Reported Pricing

    11523720008 CLARITIN 10 MG LIQUI-GEL CAP

    Pricing Unit: EA | Drug Type:

    11523720003 CLARITIN 10 MG LIQUI-GEL CAP

    Pricing Unit: EA | Drug Type:

    11523720002 CLARITIN 10 MG LIQUI-GEL CAP

    Pricing Unit: EA | Drug Type:

    11523720001 CLARITIN 10 MG LIQUI-GEL CAP

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "Claritin Liqui-Gels" or generic name "Loratadine"

    NDCBrand NameGeneric Name
    11523-7200Claritin Liqui-GelsClaritin Liqui-Gels
    11523-7333Claritin Liqui-GelsClaritin Liqui-Gels
    0363-1612allergy reliefLoratadine
    0113-7612Basic Care allergy reliefLoratadine
    0113-7500basic care childrens allergy reliefloratadine
    0113-7671Basic Care Childrens Allergy ReliefLoratadine
    0121-0849Childrens LoratadineLORATADINE
    0363-2131Childrens LoratadineLoratadine
    0363-4020CHILDRENS LORATADINE ODTLoratadine
    0363-2092Childrens Wal-itinLoratadine
    0363-2108Childrens WalitinLoratadine
    0113-0612good sense allergy reliefLoratadine
    0113-1191good sense allergy reliefloratadine
    0113-1612good sense allergy reliefLoratadine
    0113-9755good sense allergy reliefloratadine
    0113-0671Good Sense childrens allergy reliefLoratadine
    0113-1019good sense childrens allergy reliefloratadine
    0113-1719good sense childrens allergy reliefLoratadine
    0363-0858Indoor Outdoor Allergy ReliefLoratadine
    0179-8317LoratadineLoratadine
    0363-0522LoratadineLoratadine
    0363-0527LoratadineLoratadine
    0363-0752LoratadineLoratadine
    0363-9603LoratadineLoratadine
    0363-0699Wal itinLoratadine
    0363-0754Wal-itinLORATADINE
    0363-1686WAL-ITINLORATADINE
    0363-9150Wal-itinLoratadine
    0363-2085Wal-itin Allergy ReliefLoratadine

    Trademark Results [Claritin]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    CLARITIN
    CLARITIN
    86896888 not registered Dead/Abandoned
    Bayer HealthCare LLC
    2016-02-04
    CLARITIN
    CLARITIN
    85755081 4467572 Live/Registered
    BAYER HEALTHCARE LLC
    2012-10-16
    CLARITIN
    CLARITIN
    85114219 4129334 Live/Registered
    BAYER HEALTHCARE LLC
    2010-08-24
    CLARITIN
    CLARITIN
    85114214 4129333 Live/Registered
    BAYER HEALTHCARE LLC
    2010-08-24
    CLARITIN
    CLARITIN
    77802517 not registered Dead/Abandoned
    Schering Corporation
    2009-08-12
    CLARITIN
    CLARITIN
    77802516 4026607 Live/Registered
    BAYER HEALTHCARE LLC
    2009-08-12
    CLARITIN
    CLARITIN
    77802513 not registered Dead/Abandoned
    MSD CONSUMER CARE, INC.
    2009-08-12
    CLARITIN
    CLARITIN
    77802511 4019978 Live/Registered
    BAYER HEALTHCARE LLC
    2009-08-12
    CLARITIN
    CLARITIN
    77438652 3621772 Live/Registered
    BAYER HEALTHCARE LLC
    2008-04-03
    CLARITIN
    CLARITIN
    77224346 not registered Dead/Abandoned
    Schering Corporation
    2007-07-09
    CLARITIN
    CLARITIN
    77224345 not registered Dead/Abandoned
    Schering Corporation
    2007-07-09
    CLARITIN
    CLARITIN
    77222203 not registered Dead/Abandoned
    Schering Corporation
    2007-07-05
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