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    NDC 68308-0716-30 Doxycycline Hyclate 200 mg/1 Details

    Doxycycline Hyclate 200 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 68308-0716
    Product ID 68308-716_2dfd52bf-9160-40a3-bc83-231da76391db
    Associated GPIs 04000020100650
    GCN Sequence Number 070917
    GCN Sequence Number Description doxycycline hyclate TABLET DR 200 MG ORAL
    HIC3 W1C
    HIC3 Description TETRACYCLINE ANTIBIOTICS
    GCN 34586
    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 200
    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 68308-0716-30 (68308071630)

    NDC Package Code 68308-716-30
    Billing NDC 68308071630
    Package 30 TABLET, DELAYED RELEASE in 1 BOTTLE (68308-716-30)
    Marketing Start Date 2017-12-18
    NDC Exclude Flag N
    Pricing Information N/A