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    NDC 00955-1021-04 Docetaxel 80 mg/4mL Details

    Docetaxel 80 mg/4mL

    Docetaxel is a INTRAVENOUS INJECTION, SOLUTION, CONCENTRATE in the HUMAN PRESCRIPTION DRUG category. It is labeled and distributed by Winthrop U.S, a business of sanofi-aventis U.S. LLC. The primary component is DOCETAXEL.

    Product Information

    NDC 00955-1021
    Product ID 0955-1021_0beea4d6-76e2-c1d8-e063-6394a90ace94
    Associated GPIs 21500005001315
    GCN Sequence Number 066751
    GCN Sequence Number Description docetaxel VIAL 80 MG/4 ML INTRAVEN
    HIC3 V1F
    HIC3 Description ANTINEOPLASTICS,MISCELLANEOUS
    GCN 29066
    HICL Sequence Number 010280
    HICL Sequence Number Description DOCETAXEL
    Brand/Generic Generic
    Proprietary Name Docetaxel
    Proprietary Name Suffix n/a
    Non-Proprietary Name Docetaxel
    Product Type HUMAN PRESCRIPTION DRUG
    Dosage Form INJECTION, SOLUTION, CONCENTRATE
    Route INTRAVENOUS
    Active Ingredient Strength 80
    Active Ingredient Units mg/4mL
    Substance Name DOCETAXEL
    Labeler Name Winthrop U.S, a business of sanofi-aventis U.S. LLC
    Pharmaceutical Class Microtubule Inhibition [PE], Microtubule Inhibitor [EPC]
    DEA Schedule n/a
    Marketing Category NDA AUTHORIZED GENERIC
    Application Number NDA020449
    Listing Certified Through 2024-12-31

    Package

    NDC 00955-1021-04 (00955102104)

    NDC Package Code 0955-1021-04
    Billing NDC 00955102104
    Package 1 VIAL, GLASS in 1 CARTON (0955-1021-04) / 4 mL in 1 VIAL, GLASS
    Marketing Start Date 2010-10-21
    NDC Exclude Flag N
    Pricing Information N/A