NDC 62756-523

Desloratadine

Desloratadine

Desloratadine is a Oral Tablet, Film Coated in the Human Prescription Drug category. It is labeled and distributed by Sun Pharmaceutical Industries, Inc.. The primary component is Desloratadine.

Product ID62756-523_813c3d90-9952-476b-b1b9-12843f40dc83
NDC62756-523
Product TypeHuman Prescription Drug
Proprietary NameDesloratadine
Generic NameDesloratadine
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2010-11-24
Marketing CategoryANDA / ANDA
Application NumberANDA078359
Labeler NameSun Pharmaceutical Industries, Inc.
Substance NameDESLORATADINE
Active Ingredient Strength5 mg/1
Pharm ClassesHistamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]
NDC Exclude FlagN
Listing Certified Through2019-12-31

Packaging

NDC 62756-523-83

30 TABLET, FILM COATED in 1 BOTTLE (62756-523-83)
Marketing Start Date2010-11-24
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 62756-523-83 [62756052383]

Desloratadine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078359
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-11-24

NDC 62756-523-18 [62756052318]

Desloratadine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078359
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-11-24

NDC 62756-523-08 [62756052308]

Desloratadine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078359
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2010-11-24

NDC 62756-523-13 [62756052313]

Desloratadine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078359
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-11-24

NDC 62756-523-88 [62756052388]

Desloratadine TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078359
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2010-11-24

Drug Details

Active Ingredients

IngredientStrength
DESLORATADINE5 mg/1

OpenFDA Data

SPL SET ID:58ba2dc8-10c2-4532-92e2-40ec2fee3378
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 349420
  • UPC Code
  • 0362756523883
  • Pharmacological Class

    • Histamine H1 Receptor Antagonists [MoA]
    • Histamine-1 Receptor Antagonist [EPC]

    Medicade Reported Pricing

    62756052388 DESLORATADINE 5 MG TABLET

    Pricing Unit: EA | Drug Type:

    62756052313 DESLORATADINE 5 MG TABLET

    Pricing Unit: EA | Drug Type:

    NDC Crossover Matching brand name "Desloratadine" or generic name "Desloratadine"

    NDCBrand NameGeneric Name
    0378-4017Desloratadinedesloratadine
    42291-240DesloratadineDesloratadine
    50090-3975DesloratadineDesloratadine
    50090-4794DESLORATADINEDESLORATADINE
    50268-218DesloratadineDesloratadine
    51672-4159DesloratadineDesloratadine
    55111-360DesloratadineDesloratadine
    55111-551DesloratadineDesloratadine
    62250-619DesloratadineDesloratadine
    62756-523DesloratadineDesloratadine
    63629-5270DesloratadineDesloratadine
    68180-153DESLORATADINEDESLORATADINE
    69543-107DesloratadineDesloratadine
    71335-1000DESLORATADINEDESLORATADINE
    0085-1264ClarinexDesloratadine
    0085-1334ClarinexDesloratadine
    21695-815ClarinexDesloratadine
    50090-0765ClarinexDesloratadine
    78206-119ClarinexDesloratadine
    78206-188ClarinexDesloratadine

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