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    NDC 51862-0695-06 Doxycycline Hyclate 75 mg/1 Details

    Doxycycline Hyclate 75 mg/1

    Doxycycline Hyclate is a ORAL TABLET, FILM COATED 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 51862-0695
    Product ID 51862-695_ffd2c936-9b9d-b7a3-e053-6394a90af6a3
    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, FILM COATED
    Route ORAL
    Active Ingredient Strength 75
    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 ANDA
    Application Number ANDA208765
    Listing Certified Through 2024-12-31

    Package

    NDC 51862-0695-06 (51862069506)

    NDC Package Code 51862-695-06
    Billing NDC 51862069506
    Package 60 TABLET, FILM COATED in 1 BOTTLE (51862-695-06)
    Marketing Start Date 2017-06-14
    NDC Exclude Flag N
    Pricing Information N/A