Search by Drug Name or NDC

    NDC 00955-1020-01 Docetaxel 20 mg/mL Details

    Docetaxel 20 mg/mL

    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 00955-1020
    Product ID 0955-1020_0beea4d6-76e2-c1d8-e063-6394a90ace94
    Associated GPIs 21500005001310
    GCN Sequence Number 066750
    GCN Sequence Number Description docetaxel VIAL 20MG/ML(1) INTRAVEN
    HIC3 V1F
    HIC3 Description ANTINEOPLASTICS,MISCELLANEOUS
    GCN 28663
    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 20
    Active Ingredient Units mg/mL
    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 00955-1020-01 (00955102001)

    NDC Package Code 0955-1020-01
    Billing NDC 00955102001
    Package 1 VIAL, GLASS in 1 CARTON (0955-1020-01) / 1 mL in 1 VIAL, GLASS
    Marketing Start Date 2010-10-21
    NDC Exclude Flag N
    Pricing Information N/A