Search by Drug Name or NDC

    NDC 62332-0484-71 Doxycycline Hyclate 200 mg/1 Details

    Doxycycline Hyclate 200 mg/1

    Doxycycline Hyclate is a ORAL TABLET, DELAYED RELEASE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Alembic Pharmaceuticals Inc.. The primary component is DOXYCYCLINE HYCLATE.

    Product Information

    NDC 62332-0484
    Product ID 62332-484_1a84ffe4-b0ad-44df-bd67-2c752e710e42
    Associated GPIs
    GCN Sequence Number 070917
    GCN Sequence Number Description doxycycline hyclate TABLET DR 200 MG ORAL
    HIC3 W1C
    HIC3 Description TETRACYCLINE ANTIBIOTICS
    GCN 34586
    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, DELAYED RELEASE
    Route ORAL
    Active Ingredient Strength 200
    Active Ingredient Units mg/1
    Substance Name DOXYCYCLINE HYCLATE
    Labeler Name Alembic Pharmaceuticals Inc.
    Pharmaceutical Class Tetracycline-class Drug [EPC], Tetracyclines [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA213075
    Listing Certified Through 2024-12-31

    Package

    NDC 62332-0484-71 (62332048471)

    NDC Package Code 62332-484-71
    Billing NDC 62332048471
    Package 500 TABLET, DELAYED RELEASE in 1 BOTTLE (62332-484-71)
    Marketing Start Date 2022-01-04
    NDC Exclude Flag N
    Pricing Information N/A