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  5. NDC Package Code: 71288-150-95 Docetaxel Anhydrous

NDC Package 71288-150-95 Docetaxel Anhydrous

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
71288-150-95
Package Description:
1 VIAL, SINGLE-DOSE in 1 CARTON / 2 mL in 1 VIAL, SINGLE-DOSE
Product Code:
71288-150
Proprietary Name:
Docetaxel Anhydrous
Usage Information:
Docetaxel injection is contraindicated in patients with: neutrophil counts of <1500 cells/mm3 [see Warnings and Precautions (5.3)].a history of severe hypersensitivity reactions to docetaxel or to other drugs formulated with polysorbate 80. Severe reactions, including anaphylaxis, have occurred [see Warnings and Precautions (5.5)].
11-Digit NDC Billing Format:
71288015095
NDC to RxNorm Crosswalk:
  • RxCUI: 1093280 - DOCEtaxel 10 MG/ML Injectable Solution
  • RxCUI: 1093280 - docetaxel 10 MG/ML Injectable Solution
  • RxCUI: 1860619 - DOCEtaxel 20 MG in 2 ML Injection
  • RxCUI: 1860619 - 2 ML docetaxel 10 MG/ML Injection
  • RxCUI: 1860619 - docetaxel 20 MG per 2 ML Injection
    • Labeler Name:
    Meitheal Pharmaceuticals Inc
    Sample Package:
    No
    Start Marketing Date:
    08-24-2018
    Listing Expiration Date:
    12-31-2022
    Exclude Flag:
    I
    Code Structure:

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 71288-150-95?

    The NDC Packaged Code 71288-150-95 is assigned to a package of 1 vial, single-dose in 1 carton / 2 ml in 1 vial, single-dose of Docetaxel Anhydrous, labeled by Meitheal Pharmaceuticals Inc. The product's dosage form is and is administered via form.

    Is NDC 71288-150 included in the NDC Directory?

    No, Docetaxel Anhydrous with product code 71288-150 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Meitheal Pharmaceuticals Inc on August 24, 2018 and its listing in the NDC Directory is set to expire on December 31, 2022 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 71288-150-95?

    The 11-digit format is 71288015095. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-271288-150-955-4-271288-0150-95