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    NDC 70710-1122-01 Doxycycline 75 mg/1 Details

    Doxycycline 75 mg/1

    Doxycycline is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Zydus Pharmaceuticals USA Inc.. The primary component is DOXYCYCLINE.

    Product Information

    NDC 70710-1122
    Product ID 70710-1122_80bbba02-bc83-4e88-af10-fea134197df4
    Associated GPIs 04000020000307
    GCN Sequence Number 051756
    GCN Sequence Number Description doxycycline monohydrate TABLET 75 MG ORAL
    HIC3 W1C
    HIC3 Description TETRACYCLINE ANTIBIOTICS
    GCN 19107
    HICL Sequence Number 004014
    HICL Sequence Number Description DOXYCYCLINE MONOHYDRATE
    Brand/Generic Generic
    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 75
    Active Ingredient Units mg/1
    Substance Name DOXYCYCLINE
    Labeler Name Zydus Pharmaceuticals USA Inc.
    Pharmaceutical Class Tetracycline-class Drug [EPC], Tetracyclines [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA209582
    Listing Certified Through 2024-12-31

    Package

    NDC 70710-1122-01 (70710112201)

    NDC Package Code 70710-1122-1
    Billing NDC 70710112201
    Package 100 TABLET, FILM COATED in 1 BOTTLE (70710-1122-1)
    Marketing Start Date 2018-01-11
    NDC Exclude Flag N
    Pricing Information N/A