NDC 11523-7160

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 ID11523-7160_8242a0ef-e3e8-8e01-e053-2a91aa0abdc9
NDC11523-7160
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 11523-7160-1

1 BLISTER PACK in 1 CARTON (11523-7160-1) > 5 TABLET in 1 BLISTER PACK
Marketing Start Date1993-04-12
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 11523-7160-6 [11523716006]

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

NDC 11523-7160-9 [11523716009]

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

NDC 11523-7160-7 [11523716007]

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

NDC 11523-7160-8 [11523716008]

Claritin TABLET
Marketing CategoryNDA
Application NumberNDA019658
Product TypeHUMAN OTC DRUG
Marketing Start Date2016-09-01

NDC 11523-7160-2 [11523716002]

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

NDC 11523-7160-1 [11523716001]

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

NDC 11523-7160-3 [11523716003]

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

NDC 11523-7160-5 [11523716005]

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

Drug Details

Active Ingredients

IngredientStrength
LORATADINE10 mg/1

OpenFDA Data

SPL SET ID:660ac9df-f1b1-4c89-94dd-9fae0a013f3c
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 311372
  • 206805
  • UPC Code
  • 0041100808707
  • 0041100806147
  • Medicade Reported Pricing

    11523716005 CLARITIN 10 MG TABLET

    Pricing Unit: EA | Drug Type:

    11523716003 CLARITIN 10 MG TABLET

    Pricing Unit: EA | Drug Type:

    11523716002 CLARITIN 10 MG TABLET

    Pricing Unit: EA | Drug Type:

    11523716001 CLARITIN 10 MG TABLET

    Pricing Unit: EA | Drug Type: