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  5. NDC Package Code: 0143-9665-10 Cefazolin

NDC Package 0143-9665-10 Cefazolin

Injection, Powder, For Solution Intravenous - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

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:
0143-9665-10
Package Description:
1 INJECTION, POWDER, FOR SOLUTION in 1 VIAL
Product Code:
0143-9665
Proprietary Name:
Cefazolin
Non-Proprietary Name:
Cefazolin
Substance Name:
Cefazolin Sodium
Usage Information:
Cefazolin is an antibiotic used to treat a wide variety of bacterial infections. It may also be used before and during certain surgeries to help prevent infection. This medication is known as a cephalosporin antibiotic. It works by stopping the growth of bacteria.
11-Digit NDC Billing Format:
00143966510
NDC to RxNorm Crosswalk:
  • RxCUI: 313920 - ceFAZolin 200 MG/ML Injection
  • RxCUI: 313920 - cefazolin 200 MG/ML Injectable Solution
  • RxCUI: 313920 - cefazolin (as cefazolin sodium) 200 MG/ML Injectable Solution
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    West-ward Pharmaceuticals Corp
    Dosage Form:
    Injection, Powder, For Solution - A sterile preparation intended for reconstitution to form a solution for parenteral use.
    Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
    • Active Ingredient(s):
  • CEFAZOLIN SODIUM 20 g/1
    • Pharmacologic Class(es):
  • Cephalosporin Antibacterial - [EPC] (Established Pharmacologic Class)
  • Cephalosporins - [CS]
    • Sample Package:
    No
    FDA Application Number:
    ANDA065143
    Marketing Category:
    ANDA - A product marketed under an approved Abbreviated New Drug Application.
    Start Marketing Date:
    10-18-2004
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    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 0143-9665-10?

    The NDC Packaged Code 0143-9665-10 is assigned to a package of 1 injection, powder, for solution in 1 vial of Cefazolin, a human prescription drug labeled by West-ward Pharmaceuticals Corp. The product's dosage form is injection, powder, for solution and is administered via intravenous form.

    Is NDC 0143-9665 included in the NDC Directory?

    Yes, Cefazolin with product code 0143-9665 is active and included in the NDC Directory. The product was first marketed by West-ward Pharmaceuticals Corp on October 18, 2004 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 0143-9665-10?

    The 11-digit format is 00143966510. 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 4-4-2 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
    4-4-20143-9665-105-4-200143-9665-10