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    NDC 68180-0153-13 DESLORATADINE 5 mg/1 Details

    DESLORATADINE 5 mg/1

    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 Information

    NDC 68180-0153
    Product ID 68180-153_4645dca0-0380-4f47-8fd8-43c3ce8c3b71
    Associated GPIs 41550021000320
    GCN Sequence Number 047763
    GCN Sequence Number Description desloratadine TABLET 5 MG ORAL
    HIC3 Z2Q
    HIC3 Description ANTIHISTAMINES - 2ND GENERATION
    GCN 12762
    HICL Sequence Number 021934
    HICL Sequence Number Description DESLORATADINE
    Brand/Generic Generic
    Proprietary Name DESLORATADINE
    Proprietary Name Suffix n/a
    Non-Proprietary Name DESLORATADINE
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 5
    Active Ingredient Units mg/1
    Substance Name DESLORATADINE
    Labeler Name Lupin Pharmaceuticals, Inc.
    Pharmaceutical Class Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA078352
    Listing Certified Through 2025-12-31

    Package

    NDC 68180-0153-13 (68180015313)

    NDC Package Code 68180-153-13
    Billing NDC 68180015313
    Package 10 BLISTER PACK in 1 CARTON (68180-153-13) / 10 TABLET, FILM COATED in 1 BLISTER PACK (68180-153-11)
    Marketing Start Date 2013-02-25
    NDC Exclude Flag N
    Pricing Information N/A