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    NDC 51862-0696-06 Doxycycline Hyclate 150 mg/1 Details

    Doxycycline Hyclate 150 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 51862-0696
    Product ID 51862-696_ffd2c936-9b9d-b7a3-e053-6394a90af6a3
    Associated GPIs 04000020100315
    GCN Sequence Number 072634
    GCN Sequence Number Description doxycycline hyclate TABLET 150 MG ORAL
    HIC3 W1C
    HIC3 Description TETRACYCLINE ANTIBIOTICS
    GCN 36906
    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 150
    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 51862-0696-06 (51862069606)

    NDC Package Code 51862-696-06
    Billing NDC 51862069606
    Package 60 TABLET, FILM COATED in 1 BOTTLE (51862-696-06)
    Marketing Start Date 2017-06-14
    NDC Exclude Flag N
    Pricing Information N/A