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    NDC 60505-4382-06 Doxycycline Hyclate 75 mg/1 Details

    Doxycycline Hyclate 75 mg/1

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

    Product Information

    NDC 60505-4382
    Product ID 60505-4382_125cf22f-0f34-f43e-2a3e-db865e84b4e0
    Associated GPIs 04000020100307
    GCN Sequence Number 072633
    GCN Sequence Number Description doxycycline hyclate TABLET 75 MG ORAL
    HIC3 W1C
    HIC3 Description TETRACYCLINE ANTIBIOTICS
    GCN 36905
    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, COATED
    Route ORAL
    Active Ingredient Strength 75
    Active Ingredient Units mg/1
    Substance Name DOXYCYCLINE HYCLATE
    Labeler Name Apotex Corp.
    Pharmaceutical Class Tetracycline-class Drug [EPC], Tetracyclines [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA209243
    Listing Certified Through 2024-12-31

    Package

    NDC 60505-4382-06 (60505438206)

    NDC Package Code 60505-4382-6
    Billing NDC 60505438206
    Package 60 TABLET, COATED in 1 BOTTLE (60505-4382-6)
    Marketing Start Date 2019-08-01
    NDC Exclude Flag N
    Pricing Information N/A