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    NDC 51862-0571-30 Doxycycline Hyclate 80 mg/1 Details

    Doxycycline Hyclate 80 mg/1

    Doxycycline Hyclate is a ORAL TABLET, DELAYED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Mayne Pharma Commercial LLC. The primary component is DOXYCYCLINE HYCLATE.

    Product Information

    NDC 51862-0571
    Product ID 51862-571_ea09463b-6f16-4086-9290-9721fa93d666
    Associated GPIs 04000020100624
    GCN Sequence Number 079653
    GCN Sequence Number Description doxycycline hyclate TABLET DR 80 MG ORAL
    HIC3 W1C
    HIC3 Description TETRACYCLINE ANTIBIOTICS
    GCN 46194
    HICL Sequence Number 004013
    HICL Sequence Number Description DOXYCYCLINE HYCLATE
    Brand/Generic Generic
    Proprietary Name Doxycycline Hyclate
    Proprietary Name Suffix n/a
    Non-Proprietary Name Doxycycline Hyclate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, DELAYED RELEASE
    Route ORAL
    Active Ingredient Strength 80
    Active Ingredient Units mg/1
    Substance Name DOXYCYCLINE HYCLATE
    Labeler Name Mayne Pharma Commercial LLC
    Pharmaceutical Class Tetracycline-class Drug [EPC], Tetracyclines [CS]
    DEA Schedule n/a
    Marketing Category NDA AUTHORIZED GENERIC
    Application Number NDA050795
    Listing Certified Through 2024-12-31

    Package

    NDC 51862-0571-30 (51862057130)

    NDC Package Code 51862-571-30
    Billing NDC 51862057130
    Package 30 TABLET, DELAYED RELEASE in 1 BOTTLE (51862-571-30)
    Marketing Start Date 2020-10-02
    NDC Exclude Flag N
    Pricing Information N/A