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    NDC 71610-0507-53 Hydroxychloroquine Sulfate 200 mg/1 Details

    Hydroxychloroquine Sulfate 200 mg/1

    Hydroxychloroquine Sulfate is a ORAL TABLET, FILM COATED in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Aphena Pharma Solutions - Tennessee, LLC. The primary component is HYDROXYCHLOROQUINE SULFATE.

    Product Information

    NDC 71610-0507
    Product ID 71610-507_eaefffa9-a606-427c-bda6-441db98954b9
    Associated GPIs 13000020100305
    GCN Sequence Number 009580
    GCN Sequence Number Description hydroxychloroquine sulfate TABLET 200 MG ORAL
    HIC3 W4A
    HIC3 Description ANTIMALARIAL DRUGS
    GCN 42940
    HICL Sequence Number 004151
    HICL Sequence Number Description HYDROXYCHLOROQUINE SULFATE
    Brand/Generic Generic
    Proprietary Name Hydroxychloroquine Sulfate
    Proprietary Name Suffix n/a
    Non-Proprietary Name Hydroxychloroquine Sulfate
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 200
    Active Ingredient Units mg/1
    Substance Name HYDROXYCHLOROQUINE SULFATE
    Labeler Name Aphena Pharma Solutions - Tennessee, LLC
    Pharmaceutical Class Antimalarial [EPC], Antirheumatic Agent [EPC]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA040274
    Listing Certified Through 2023-12-31

    Package

    NDC 71610-0507-53 (71610050753)

    NDC Package Code 71610-507-53
    Billing NDC 71610050753
    Package 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71610-507-53)
    Marketing Start Date 2020-12-21
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 953b84b4-5b83-4b47-a068-7382c2c090e7 Details

    Revised: 12/2020