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    NDC 23155-0611-06 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 Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.. The primary component is DOXYCYCLINE HYCLATE.

    Product Information

    NDC 23155-0611
    Product ID 23155-611_599f2c2d-dcd8-4e17-a2a8-2266ac4a8a56
    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 DELAYED RELEASE
    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 Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.
    Pharmaceutical Class Tetracycline-class Drug [EPC], Tetracyclines [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA200856
    Listing Certified Through 2024-12-31

    Package

    NDC 23155-0611-06 (23155061106)

    NDC Package Code 23155-611-06
    Billing NDC 23155061106
    Package 60 TABLET, DELAYED RELEASE in 1 BOTTLE (23155-611-06)
    Marketing Start Date 2018-03-16
    NDC Exclude Flag N
    Pricing Information N/A