NDC 68180-153

DESLORATADINE

Desloratadine

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

Product ID68180-153_6099aa30-f7c1-43e9-b3fc-650bb0241861
NDC68180-153
Product TypeHuman Prescription Drug
Proprietary NameDESLORATADINE
Generic NameDesloratadine
Dosage FormTablet, Film Coated
Route of AdministrationORAL
Marketing Start Date2013-02-25
Marketing CategoryANDA / ANDA
Application NumberANDA078352
Labeler NameLupin Pharmaceuticals, Inc.
Substance NameDESLORATADINE
Active Ingredient Strength5 mg/1
Pharm ClassesHistamine H1 Receptor Antagonists [MoA],Histamine-1 Receptor Antagonist [EPC]
NDC Exclude FlagN
Listing Certified Through2021-12-31

Packaging

NDC 68180-153-01

100 TABLET, FILM COATED in 1 BOTTLE (68180-153-01)
Marketing Start Date2013-02-25
NDC Exclude FlagN
Sample Package?N

NDC SPL Data Element Entries

NDC 68180-153-06 [68180015306]

DESLORATADINE TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078352
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-02-25

NDC 68180-153-02 [68180015302]

DESLORATADINE TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078352
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2013-02-25

NDC 68180-153-13 [68180015313]

DESLORATADINE TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078352
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-02-25

NDC 68180-153-01 [68180015301]

DESLORATADINE TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078352
Product TypeHUMAN PRESCRIPTION DRUG
Billing UnitEA
Marketing Start Date2013-02-25

NDC 68180-153-11 [68180015311]

DESLORATADINE TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078352
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-02-25

NDC 68180-153-12 [68180015312]

DESLORATADINE TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078352
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-02-25

NDC 68180-153-03 [68180015303]

DESLORATADINE TABLET, FILM COATED
Marketing CategoryANDA
Application NumberANDA078352
Product TypeHUMAN PRESCRIPTION DRUG
Marketing Start Date2013-02-25

Drug Details

Active Ingredients

IngredientStrength
DESLORATADINE5 mg/1

OpenFDA Data

SPL SET ID:2a90b899-7746-43dc-ac8a-e754428eb30c
Manufacturer
UNII
RxNorm Concept Unique ID - RxCUI
  • 349420
    • UPC Code
  • 0368180153016

    • Pharmacological Class

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

    Medicade Reported Pricing

    68180015302 DESLORATADINE 5 MG TABLET

    Pricing Unit: EA | Drug Type:

    68180015301 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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