NDC 49348-818

Sunmark Loratadine

Loratadine

Sunmark Loratadine is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Mckesson. The primary component is Loratadine.

Product ID49348-818_12557a59-3e24-4b39-9fbf-17461a49ec10
NDC49348-818
Product TypeHuman Otc Drug
Proprietary NameSunmark Loratadine
Generic NameLoratadine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2007-06-21
Marketing CategoryANDA / ANDA
Application NumberANDA076301
Labeler NameMcKesson
Substance NameLORATADINE
Active Ingredient Strength10 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 49348-818-01

10 BLISTER PACK in 1 CARTON (49348-818-01) > 1 TABLET in 1 BLISTER PACK
Marketing Start Date2007-06-25
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 49348-818-45 [49348081845]

Sunmark Loratadine TABLET
Marketing CategoryANDA
Application NumberANDA076301
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2018-10-24

NDC 49348-818-56 [49348081856]

Sunmark Loratadine TABLET
Marketing CategoryANDA
Application NumberANDA076301
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2014-03-31

NDC 49348-818-12 [49348081812]

Sunmark Loratadine TABLET
Marketing CategoryANDA
Application NumberANDA076301
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2007-07-13
Marketing End Date2015-06-07

NDC 49348-818-44 [49348081844]

Sunmark Loratadine TABLET
Marketing CategoryANDA
Application NumberANDA076301
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2007-06-21

NDC 49348-818-13 [49348081813]

Sunmark Loratadine TABLET
Marketing CategoryANDA
Application NumberANDA076301
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2007-06-21

NDC 49348-818-01 [49348081801]

Sunmark Loratadine TABLET
Marketing CategoryANDA
Application NumberANDA076301
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2007-06-25

Drug Details

Active Ingredients

IngredientStrength
LORATADINE10 mg/1

OpenFDA Data

SPL SET ID:d17f1c32-095c-48e9-acc5-d5b94571b9b4
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 311372

    • Medicade Reported Pricing

    49348081856 SM LORATADINE 10 MG TABLET

    Pricing Unit: EA | Drug Type:

    49348081844 SM LORATADINE 10 MG TABLET

    Pricing Unit: EA | Drug Type:

    49348081813 SM LORATADINE 10 MG TABLET

    Pricing Unit: EA | Drug Type:

    49348081812 SM LORATADINE 10 MG TABLET

    Pricing Unit: EA | Drug Type:

    49348081801 SM LORATADINE 10 MG TABLET

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "Sunmark Loratadine" or generic name "Loratadine"

    NDCBrand NameGeneric Name
    49348-394SUNMARK LORATADINESUNMARK LORATADINE
    49348-818Sunmark LoratadineSunmark Loratadine
    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
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