NDC 51660-526

Loratadine Allergy Relief

Loratadine

Loratadine Allergy Relief is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Ohm Laboratories Inc.. The primary component is Loratadine.

Product ID51660-526_3b691f3e-8ec9-45f2-880b-c35fd9fb3a62
NDC51660-526
Product TypeHuman Otc Drug
Proprietary NameLoratadine Allergy Relief
Generic NameLoratadine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2017-11-01
Marketing CategoryANDA / ANDA
Application NumberANDA076134
Labeler NameOHM LABORATORIES INC.
Substance NameLORATADINE
Active Ingredient Strength10 mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 51660-526-01

100 TABLET in 1 BOTTLE (51660-526-01)
Marketing Start Date2017-11-01
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 51660-526-01 [51660052601]

Loratadine Allergy Relief TABLET
Marketing CategoryANDA
Application NumberANDA076134
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2017-11-01

NDC 51660-526-05 [51660052605]

Loratadine Allergy Relief TABLET
Marketing CategoryANDA
Application NumberANDA076134
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2017-11-01

NDC 51660-526-31 [51660052631]

Loratadine Allergy Relief TABLET
Marketing CategoryANDA
Application NumberANDA076134
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2017-11-01

NDC 51660-526-60 [51660052660]

Loratadine Allergy Relief TABLET
Marketing CategoryANDA
Application NumberANDA076134
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-11-01
Marketing End Date2017-12-31

NDC 51660-526-53 [51660052653]

Loratadine Allergy Relief TABLET
Marketing CategoryANDA
Application NumberANDA076134
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2017-11-01

NDC 51660-526-30 [51660052630]

Loratadine Allergy Relief TABLET
Marketing CategoryANDA
Application NumberANDA076134
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2019-02-01

NDC 51660-526-11 [51660052611]

Loratadine Allergy Relief TABLET
Marketing CategoryANDA
Application NumberANDA076134
Product TypeHUMAN OTC DRUG
Marketing Start Date2017-11-01
Marketing End Date2017-12-31

Drug Details

Active Ingredients

IngredientStrength
LORATADINE10 mg/1

OpenFDA Data

SPL SET ID:c35f2cc1-f76d-4824-b0a5-747bca0c3b85
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 311372
  • Medicade Reported Pricing

    51660052653 ALLERGY RELIEF 10 MG TABLET

    Pricing Unit: EA | Drug Type:

    51660052631 LORATADINE 10 MG TABLET

    Pricing Unit: EA | Drug Type:

    51660052628 LORATADINE 10 MG TABLET

    Pricing Unit: EA | Drug Type:

    51660052611 ALLERGY (LORATADINE) 10 MG TAB

    Pricing Unit: EA | Drug Type:

    51660052605 LORATADINE 10 MG TABLET

    Pricing Unit: EA | Drug Type:

    51660052601 LORATADINE 10 MG TABLET

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "Loratadine Allergy Relief" or generic name "Loratadine"

    NDCBrand NameGeneric Name
    68071-3208Loratadine Allergy ReliefLoratadine Allergy Relief
    68071-4788Loratadine Allergy ReliefLoratadine Allergy Relief
    70518-1399Loratadine Allergy ReliefLoratadine Allergy Relief
    70934-205Loratadine Allergy ReliefLoratadine Allergy Relief
    71141-132Loratadine Allergy ReliefLoratadine Allergy Relief
    71335-0100Loratadine Allergy ReliefLoratadine Allergy Relief
    37808-529Loratadine Allergy ReliefLoratadine Allergy Relief
    50090-2387Loratadine Allergy ReliefLoratadine Allergy Relief
    51660-526Loratadine Allergy ReliefLoratadine Allergy Relief
    53002-7490Loratadine Allergy ReliefLoratadine Allergy Relief
    53943-975Loratadine Allergy ReliefLoratadine Allergy Relief
    55289-728Loratadine Allergy ReliefLoratadine Allergy Relief
    55700-097Loratadine Allergy ReliefLoratadine Allergy Relief
    63187-100Loratadine Allergy ReliefLoratadine Allergy Relief
    63629-7772Loratadine Allergy ReliefLoratadine Allergy Relief
    64725-0526Loratadine Allergy ReliefLoratadine Allergy Relief
    67046-452Loratadine Allergy ReliefLoratadine Allergy Relief
    67091-246Loratadine Allergy ReliefLoratadine Allergy Relief
    67091-245Loratadine Allergy ReliefLoratadine Allergy Relief
    68071-4910Loratadine Allergy ReliefLoratadine Allergy Relief
    68071-5049Loratadine Allergy ReliefLoratadine Allergy Relief
    68788-7482Loratadine Allergy ReliefLoratadine Allergy Relief
    70934-779Loratadine Allergy ReliefLoratadine Allergy Relief
    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

    © 2024 FDA.report
    This site is not affiliated with or endorsed by the FDA.