NDC 21130-527

Loratadine ODT

Loratadine

Loratadine ODT is a Oral Tablet, Orally Disintegrating in the Human Otc Drug category. It is labeled and distributed by Safeway Inc.. The primary component is Loratadine.

Product ID21130-527_d5ec9af0-b2a0-47cd-a418-cfc00df2afd8
NDC21130-527
Product TypeHuman Otc Drug
Proprietary NameLoratadine ODT
Generic NameLoratadine
Dosage FormTablet, Orally Disintegrating
Route of AdministrationORAL
Marketing Start Date2007-08-31
Marketing CategoryANDA / ANDA
Application NumberANDA077153
Labeler NameSafeway Inc.
Substance NameLORATADINE
Active Ingredient Strength10 mg/1
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 21130-527-69

10 TABLET, ORALLY DISINTEGRATING in 1 BLISTER PACK (21130-527-69)
Marketing Start Date2007-08-31
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 21130-527-69 [21130052769]

Loratadine ODT TABLET, ORALLY DISINTEGRATING
Marketing CategoryANDA
Application NumberANDA077153
Product TypeHUMAN OTC DRUG
Marketing Start Date2007-08-31
Inactivation Date2020-01-31

NDC 21130-527-31 [21130052731]

Loratadine ODT TABLET, ORALLY DISINTEGRATING
Marketing CategoryANDA
Application NumberANDA077153
Product TypeHUMAN OTC DRUG
Marketing Start Date2007-08-31
Inactivation Date2020-01-31

Drug Details

Active Ingredients

IngredientStrength
LORATADINE10 mg/1

OpenFDA Data

SPL SET ID:244e041f-20e2-4e38-ac6b-bf96f8724d5e
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 311373
    • UPC Code
  • 0321130762409

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

    NDCBrand NameGeneric Name
    68016-088Loratadine ODTLoratadine ODT
    68016-527Loratadine ODTLoratadine ODT
    69842-085Loratadine ODTLoratadine ODT
    0904-5806Loratadine ODTLoratadine ODT
    21130-527Loratadine ODTLoratadine ODT
    36800-528Loratadine ODTLoratadine ODT
    37012-527Loratadine ODTLoratadine ODT
    41250-527Loratadine ODTLoratadine ODT
    41250-513Loratadine ODTLoratadine ODT
    46122-539Loratadine ODTLoratadine ODT
    49035-806Loratadine ODTLoratadine ODT
    53943-035Loratadine ODTLoratadine ODT
    58602-744Loratadine ODTLoratadine ODT
    58602-821Loratadine ODTLoratadine ODT
    58602-830Loratadine ODTLoratadine ODT
    59779-527Loratadine ODTLoratadine ODT
    60000-950Loratadine ODTLoratadine ODT
    0363-9937Loratadine ODTLoratadine ODT
    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 [Loratadine ODT]

    Mark Image

    Registration | Serial
    Company
    Trademark
    Application Date
    LORATADINE ODT
    LORATADINE ODT
    76601213 not registered Dead/Abandoned
    LEINER HEALTH SERVICES CORP.
    2004-07-08
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