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    NDC 63629-2285-01 Tretinoin 10 mg/1 Details

    Tretinoin 10 mg/1

    Tretinoin is a ORAL CAPSULE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Bryant Ranch Prepack. The primary component is TRETINOIN.

    Product Information

    NDC 63629-2285
    Product ID 63629-2285_2294c670-ded9-47b9-ae22-9807039077a9
    Associated GPIs 21708080000110
    GCN Sequence Number 024466
    GCN Sequence Number Description tretinoin CAPSULE 10 MG ORAL
    HIC3 V1F
    HIC3 Description ANTINEOPLASTICS,MISCELLANEOUS
    GCN 48590
    HICL Sequence Number 002468
    HICL Sequence Number Description TRETINOIN
    Brand/Generic Generic
    Proprietary Name Tretinoin
    Proprietary Name Suffix n/a
    Non-Proprietary Name Tretinoin
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form CAPSULE
    Route ORAL
    Active Ingredient Strength 10
    Active Ingredient Units mg/1
    Substance Name TRETINOIN
    Labeler Name Bryant Ranch Prepack
    Pharmaceutical Class Retinoid [EPC], Retinoids [CS]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA201687
    Listing Certified Through 2025-12-31

    Package

    NDC 63629-2285-01 (63629228501)

    NDC Package Code 63629-2285-1
    Billing NDC 63629228501
    Package 100 CAPSULE in 1 BOTTLE (63629-2285-1)
    Marketing Start Date 2021-03-29
    NDC Exclude Flag N
    Pricing Information N/A