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    NDC 51655-0998-53 Doxycycline 100 mg/1 Details

    Doxycycline 100 mg/1

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

    Product Information

    NDC 51655-0998
    Product ID 51655-998_fe070e2e-3e75-fb84-e053-6294a90afd88
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Doxycycline
    Proprietary Name Suffix n/a
    Non-Proprietary Name Doxycycline hyclate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, COATED
    Route ORAL
    Active Ingredient Strength 100
    Active Ingredient Units mg/1
    Substance Name DOXYCYCLINE HYCLATE
    Labeler Name Northwind Pharmaceuticals, LLC
    Pharmaceutical Class Tetracycline-class Drug [EPC], Tetracyclines [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA065095
    Listing Certified Through 2024-12-31

    Package

    NDC 51655-0998-53 (51655099853)

    NDC Package Code 51655-998-53
    Billing NDC 51655099853
    Package 10 TABLET, COATED in 1 BOTTLE, PLASTIC (51655-998-53)
    Marketing Start Date 2023-06-08
    NDC Exclude Flag N
    Pricing Information N/A