NDC 41163-612

Equaline Allergy Relief

Loratadine

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

Product ID41163-612_00620642-2b87-4f53-bc51-398f36e91f37
NDC41163-612
Product TypeHuman Otc Drug
Proprietary NameEqualine Allergy Relief
Generic NameLoratadine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2005-02-07
Marketing CategoryANDA / ANDA
Application NumberANDA076301
Labeler NameSupervalu Inc
Substance NameLORATADINE
Active Ingredient Strength10 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 41163-612-46

10 BLISTER PACK in 1 CARTON (41163-612-46) > 1 TABLET in 1 BLISTER PACK
Marketing Start Date2005-02-07
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 41163-612-72 [41163061272]

Equaline Allergy Relief TABLET
Marketing CategoryANDA
Application NumberANDA076301
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2005-03-23

NDC 41163-612-58 [41163061258]

Equaline Allergy Relief TABLET
Marketing CategoryANDA
Application NumberANDA076301
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-10-03

NDC 41163-612-95 [41163061295]

Equaline Allergy Relief TABLET
Marketing CategoryANDA
Application NumberANDA076301
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2009-08-31
Marketing End Date2012-06-17

NDC 41163-612-60 [41163061260]

Equaline Allergy Relief TABLET
Marketing CategoryANDA
Application NumberANDA076301
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2005-02-08
Marketing End Date2011-11-11

NDC 41163-612-65 [41163061265]

Equaline Allergy Relief TABLET
Marketing CategoryANDA
Application NumberANDA076301
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2005-02-15

NDC 41163-612-46 [41163061246]

Equaline Allergy Relief TABLET
Marketing CategoryANDA
Application NumberANDA076301
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2005-02-07

NDC 41163-612-75 [41163061275]

Equaline Allergy Relief TABLET
Marketing CategoryANDA
Application NumberANDA076301
Product TypeHUMAN OTC DRUG
Billing UnitEA
Marketing Start Date2005-03-21

Drug Details

Active Ingredients

IngredientStrength
LORATADINE10 mg/1

OpenFDA Data

SPL SET ID:232053f0-737b-46b0-959f-9edb26d82cbf
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 311372
  • NDC Crossover Matching brand name "Equaline Allergy Relief" or generic name "Loratadine"

    NDCBrand NameGeneric Name
    41163-612Equaline Allergy ReliefEqualine 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

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