NDC 11523-6655

Claritin

Loratadine

Claritin is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Bayer Healthcare Llc. The primary component is Loratadine.

Product ID11523-6655_55ed2b95-2fbc-1c9f-e054-00144ff8d46c
NDC11523-6655
Product TypeHuman Otc Drug
Proprietary NameClaritin
Generic NameLoratadine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date1993-04-12
Marketing CategoryNDA / NDA
Application NumberNDA019658
Labeler NameBayer HealthCare LLC
Substance NameLORATADINE
Active Ingredient Strength10 mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 11523-6655-1

1 BLISTER PACK in 1 POUCH (11523-6655-1) > 1 TABLET in 1 BLISTER PACK
Marketing Start Date1993-04-12
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 11523-6655-8 [11523665508]

Claritin TABLET
Marketing CategoryNDA
Application NumberNDA019658
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date1993-04-12

NDC 11523-6655-7 [11523665507]

Claritin TABLET
Marketing CategoryNDA
Application NumberNDA019658
Product TypeHUMAN OTC DRUG
Marketing Start Date1993-04-12

NDC 11523-6655-2 [11523665502]

Claritin TABLET
Marketing CategoryNDA
Application NumberNDA019658
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date1993-04-12

NDC 11523-6655-9 [11523665509]

Claritin TABLET
Marketing CategoryNDA
Application NumberNDA019658
Product TypeHUMAN OTC DRUG
Marketing Start Date1993-04-12

NDC 11523-6655-1 [11523665501]

Claritin TABLET
Marketing CategoryNDA
Application NumberNDA019658
Product TypeHUMAN OTC DRUG
Marketing Start Date1993-04-12

NDC 11523-6655-6 [11523665506]

Claritin TABLET
Marketing CategoryNDA
Application NumberNDA019658
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date1993-04-12

NDC 11523-6655-4 [11523665504]

Claritin TABLET
Marketing CategoryNDA
Application NumberNDA019658
Product TypeHUMAN OTC DRUG
Marketing Start Date1993-04-12

NDC 11523-6655-3 [11523665503]

Claritin TABLET
Marketing CategoryNDA
Application NumberNDA019658
Product TypeHUMAN OTC DRUG
Marketing Start Date1993-04-12

NDC 11523-6655-5 [11523665505]

Claritin TABLET
Marketing CategoryNDA
Application NumberNDA019658
Product TypeHUMAN OTC DRUG
Marketing Start Date1993-04-12

Drug Details

Active Ingredients

IngredientStrength
LORATADINE10 mg/1

OpenFDA Data

SPL SET ID:ac32d6f9-f553-4d5c-ad36-575af5ea56de
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 311372
  • 206805
    • UPC Code
  • 0041100809643

    • NDC Crossover Matching brand name "Claritin" or generic name "Loratadine"

    NDCBrand NameGeneric Name
    67751-153ClaritinClaritin
    11523-7160ClaritinClaritin
    11523-7237ClaritinClaritin
    11523-4330ClaritinClaritin
    11523-4328ClaritinClaritin
    11523-4331ClaritinClaritin
    11523-4359ClaritinClaritin
    11523-1527ClaritinClaritin
    11523-6655ClaritinClaritin
    73097-005ClaritinClaritin
    11523-0007ClaritinClaritin
    70518-2951ClaritinClaritin
    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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