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    NDC 53489-0120-01 Doxycycline Hyclate 100 mg/1 Details

    Doxycycline Hyclate 100 mg/1

    Doxycycline Hyclate is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Sun Pharmaceutical Industries, Inc.. The primary component is DOXYCYCLINE HYCLATE.

    Product Information

    NDC 53489-0120
    Product ID 53489-120_0bc66ce8-33fd-5416-e063-6394a90acc50
    Associated GPIs 04000020100310
    GCN Sequence Number 009223
    GCN Sequence Number Description doxycycline hyclate TABLET 100 MG ORAL
    HIC3 W1C
    HIC3 Description TETRACYCLINE ANTIBIOTICS
    GCN 40360
    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 100
    Active Ingredient Units mg/1
    Substance Name DOXYCYCLINE HYCLATE
    Labeler Name Sun Pharmaceutical Industries, Inc.
    Pharmaceutical Class Tetracycline-class Drug [EPC], Tetracyclines [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA062677
    Listing Certified Through 2024-12-31

    Package

    NDC 53489-0120-01 (53489012001)

    NDC Package Code 53489-120-01
    Billing NDC 53489012001
    Package 100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (53489-120-01)
    Marketing Start Date 2023-12-05
    NDC Exclude Flag N
    Pricing Information N/A