NDC 58602-702

Loratadine

Loratadine

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

Product ID58602-702_282e0034-22a5-4ad3-913a-62268a36c1d2
NDC58602-702
Product TypeHuman Otc Drug
Proprietary NameLoratadine
Generic NameLoratadine
Dosage FormTablet
Route of AdministrationORAL
Marketing Start Date2018-04-16
Marketing CategoryANDA / ANDA
Application NumberANDA208314
Labeler NameAurohealth LLC
Substance NameLORATADINE
Active Ingredient Strength10 mg/1
NDC Exclude FlagN
Listing Certified Through2020-12-31

Packaging

NDC 58602-702-04

10 BLISTER PACK in 1 CARTON (58602-702-04) > 10 TABLET in 1 BLISTER PACK
Marketing Start Date2020-02-10
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 58602-702-44 [58602070244]

Loratadine TABLET
Marketing CategoryANDA
Application NumberANDA208314
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-07-26

NDC 58602-702-84 [58602070284]

Loratadine TABLET
Marketing CategoryANDA
Application NumberANDA208314
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-04-16

NDC 58602-702-15 [58602070215]

Loratadine TABLET
Marketing CategoryANDA
Application NumberANDA208314
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-04-16

NDC 58602-702-40 [58602070240]

Loratadine TABLET
Marketing CategoryANDA
Application NumberANDA208314
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-11-28

NDC 58602-702-83 [58602070283]

Loratadine TABLET
Marketing CategoryANDA
Application NumberANDA208314
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-04-16

NDC 58602-702-21 [58602070221]

Loratadine TABLET
Marketing CategoryANDA
Application NumberANDA208314
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-12-23

NDC 58602-702-67 [58602070267]

Loratadine TABLET
Marketing CategoryANDA
Application NumberANDA208314
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-04-16

NDC 58602-702-32 [58602070232]

Loratadine TABLET
Marketing CategoryANDA
Application NumberANDA208314
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-04-16

NDC 58602-702-05 [58602070205]

Loratadine TABLET
Marketing CategoryANDA
Application NumberANDA208314
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-04-16

NDC 58602-702-04 [58602070204]

Loratadine TABLET
Marketing CategoryANDA
Application NumberANDA208314
Product TypeHUMAN OTC DRUG
Marketing Start Date2020-02-10

NDC 58602-702-23 [58602070223]

Loratadine TABLET
Marketing CategoryANDA
Application NumberANDA208314
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-10-04

NDC 58602-702-60 [58602070260]

Loratadine TABLET
Marketing CategoryANDA
Application NumberANDA208314
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-04-16

NDC 58602-702-81 [58602070281]

Loratadine TABLET
Marketing CategoryANDA
Application NumberANDA208314
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-04-16

NDC 58602-702-19 [58602070219]

Loratadine TABLET
Marketing CategoryANDA
Application NumberANDA208314
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-04-16

NDC 58602-702-17 [58602070217]

Loratadine TABLET
Marketing CategoryANDA
Application NumberANDA208314
Product TypeHUMAN OTC DRUG
Marketing Start Date2018-04-16

NDC 58602-702-38 [58602070238]

Loratadine TABLET
Marketing CategoryANDA
Application NumberANDA208314
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-05-03

NDC 58602-702-39 [58602070239]

Loratadine TABLET
Marketing CategoryANDA
Application NumberANDA208314
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-05-03

NDC 58602-702-54 [58602070254]

Loratadine TABLET
Marketing CategoryANDA
Application NumberANDA208314
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-10-04

NDC 58602-702-09 [58602070209]

Loratadine TABLET
Marketing CategoryANDA
Application NumberANDA208314
Product TypeHUMAN OTC DRUG
Marketing Start Date2019-05-03

Drug Details

Active Ingredients

IngredientStrength
LORATADINE10 mg/1

OpenFDA Data

SPL SET ID:196da80c-3dbb-40c7-ac93-8a57d6acb1c3
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 311372
    • UPC Code
  • 0358602702175

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

    NDCBrand NameGeneric Name
    0179-8317LoratadineLoratadine
    0363-0522LoratadineLoratadine
    0363-0527LoratadineLoratadine
    0363-0752LoratadineLoratadine
    0363-9603LoratadineLoratadine
    68016-094LoratadineLoratadine
    68016-526LoratadineLoratadine
    68071-4121LoratadineLoratadine
    68071-3203LoratadineLoratadine
    68071-4451LoratadineLoratadine
    68084-248LoratadineLoratadine
    68788-7085LORATADINELORATADINE
    68788-7291LoratadineLoratadine
    68788-9805LoratadineLoratadine
    0536-1092LORATADINELORATADINE
    69452-211LORATADINELORATADINE
    69842-686LORATADINELORATADINE
    70000-0317LORATADINELORATADINE
    70000-0217LORATADINELORATADINE
    70000-0125LoratadineLoratadine
    70518-0325LoratadineLoratadine
    70518-1262LORATADINELORATADINE
    71335-0751LoratadineLoratadine
    71335-0888LoratadineLoratadine
    0615-5586LoratadineLoratadine
    0781-5077LoratadineLoratadine
    0904-5793LORATADINELORATADINE
    0904-6074LoratadineLoratadine
    0904-6234LoratadineLoratadine
    0904-6852LoratadineLoratadine
    10544-455LoratadineLoratadine
    11673-513LoratadineLoratadine
    11673-527LoratadineLoratadine
    11822-7240LORATADINELORATADINE
    15127-715LoratadineLoratadine
    15127-979LoratadineLoratadine
    16714-482LoratadineLoratadine
    17856-6234LoratadineLoratadine
    16714-898LoratadineLoratadine
    21130-526LoratadineLoratadine
    21695-499LoratadineLoratadine
    17856-0557LoratadineLoratadine
    21695-498LoratadineLoratadine
    24385-540LoratadineLoratadine
    25000-021loratadineloratadine
    24385-161LoratadineLoratadine
    36800-527LoratadineLoratadine
    37205-378LoratadineLoratadine
    37012-526LoratadineLoratadine
    41163-528LoratadineLoratadine
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