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    NDC 69238-1754-06 ABIRATERONE ACETATE 500 mg/1 Details

    ABIRATERONE ACETATE 500 mg/1

    ABIRATERONE ACETATE is a ORAL TABLET in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Amneal Pharmaceuticals NY LLC. The primary component is ABIRATERONE ACETATE.

    Product Information

    NDC 69238-1754
    Product ID 69238-1754_c03e6ebe-681b-40c0-b123-741dd35fd558
    Associated GPIs 21406010200330
    GCN Sequence Number 077249
    GCN Sequence Number Description abiraterone acetate TABLET 500 MG ORAL
    HIC3 V1J
    HIC3 Description ANTINEOPLASTIC - ANTIANDROGENIC AGENTS
    GCN 43205
    HICL Sequence Number 037571
    HICL Sequence Number Description ABIRATERONE ACETATE
    Brand/Generic Generic
    Proprietary Name ABIRATERONE ACETATE
    Proprietary Name Suffix n/a
    Non-Proprietary Name ABIRATERONE
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 500
    Active Ingredient Units mg/1
    Substance Name ABIRATERONE ACETATE
    Labeler Name Amneal Pharmaceuticals NY LLC
    Pharmaceutical Class Cytochrome P450 17A1 Inhibitor [EPC], Cytochrome P450 17A1 Inhibitors [MoA], Cytochrome P450 2C8 Inhibitors [MoA], Cytochrome P450 2D6 Inhibitors [MoA]
    DEA Schedule n/a
    Marketing Category ANDA
    Application Number ANDA208327
    Listing Certified Through 2024-12-31

    Package

    NDC 69238-1754-06 (69238175406)

    NDC Package Code 69238-1754-6
    Billing NDC 69238175406
    Package 60 TABLET in 1 BOTTLE (69238-1754-6)
    Marketing Start Date 2019-01-07
    NDC Exclude Flag N
    Pricing Information N/A