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    NDC 60219-2132-01 doxycycline hyclate 100 mg/1 Details

    doxycycline hyclate 100 mg/1

    doxycycline hyclate is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Amneal Pharmaceuticals NY LLC. The primary component is DOXYCYCLINE HYCLATE.

    Product Information

    NDC 60219-2132
    Product ID 60219-2132_d003a652-9c70-4580-9d06-d7390398d399
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name doxycycline hyclate
    Proprietary Name Suffix n/a
    Non-Proprietary Name doxycycline hyclate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 100
    Active Ingredient Units mg/1
    Substance Name DOXYCYCLINE HYCLATE
    Labeler Name Amneal Pharmaceuticals NY LLC
    Pharmaceutical Class Tetracycline-class Drug [EPC], Tetracyclines [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA216599
    Listing Certified Through 2024-12-31

    Package

    NDC 60219-2132-01 (60219213201)

    NDC Package Code 60219-2132-1
    Billing NDC 60219213201
    Package 100 TABLET, FILM COATED in 1 BOTTLE (60219-2132-1)
    Marketing Start Date 2022-11-09
    NDC Exclude Flag N
    Pricing Information N/A