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    NDC 70518-3039-00 Doxycycline 100 mg/1 Details

    Doxycycline 100 mg/1

    Doxycycline is a ORAL TABLET, COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is DOXYCYCLINE HYCLATE.

    Product Information

    NDC 70518-3039
    Product ID 70518-3039_0c673104-4e84-e749-e063-6394a90a3b22
    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
    Proprietary Name Suffix n/a
    Non-Proprietary Name Doxycycline hyclate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, COATED
    Route ORAL
    Active Ingredient Strength 100
    Active Ingredient Units mg/1
    Substance Name DOXYCYCLINE HYCLATE
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Tetracycline-class Drug [EPC], Tetracyclines [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA065095
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-3039-00 (70518303900)

    NDC Package Code 70518-3039-0
    Billing NDC 70518303900
    Package 14 TABLET, COATED in 1 BOTTLE, PLASTIC (70518-3039-0)
    Marketing Start Date 2021-03-04
    NDC Exclude Flag N
    Pricing Information N/A