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    NDC 70518-3233-00 TRETINOIN 1 mg/g Details

    TRETINOIN 1 mg/g

    TRETINOIN is a TOPICAL CREAM in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by REMEDYREPACK INC.. The primary component is TRETINOIN.

    Product Information

    NDC 70518-3233
    Product ID 70518-3233_0670e4b8-34a1-5c31-e063-6394a90a6718
    Associated GPIs
    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 TRETINOIN
    Proprietary Name Suffix n/a
    Non-Proprietary Name tretinoin
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CREAM
    Route TOPICAL
    Active Ingredient Strength 1
    Active Ingredient Units mg/g
    Substance Name TRETINOIN
    Labeler Name REMEDYREPACK INC.
    Pharmaceutical Class Retinoid [EPC], Retinoids [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA075213
    Listing Certified Through 2024-12-31

    Package

    NDC 70518-3233-00 (70518323300)

    NDC Package Code 70518-3233-0
    Billing NDC 70518323300
    Package 1 TUBE in 1 CARTON (70518-3233-0) / 20 g in 1 TUBE
    Marketing Start Date 2021-10-11
    NDC Exclude Flag N
    Pricing Information N/A