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    NDC 50090-3809-00 Doxycycline 100 mg/1 Details

    Doxycycline 100 mg/1

    Doxycycline is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by A-S Medication Solutions. The primary component is DOXYCYCLINE.

    Product Information

    NDC 50090-3809
    Product ID 50090-3809_e226e0f6-37f7-4967-b524-e69835eeee6c
    Associated GPIs 04000020000310
    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
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 100
    Active Ingredient Units mg/1
    Substance Name DOXYCYCLINE
    Labeler Name A-S Medication Solutions
    Pharmaceutical Class Tetracycline-class Drug [EPC], Tetracyclines [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA209582
    Listing Certified Through 2025-12-31

    Package

    NDC 50090-3809-00 (50090380900)

    NDC Package Code 50090-3809-0
    Billing NDC 50090380900
    Package 20 TABLET, FILM COATED in 1 BOTTLE (50090-3809-0)
    Marketing Start Date 2018-11-12
    NDC Exclude Flag N
    Pricing Information N/A