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  5. NDC Package Code: 0143-9474-10 Vancomycin Hydrochloride

NDC Package 0143-9474-10 Vancomycin Hydrochloride

Injection, Powder, For Solution Intravenous; Oral - 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:
0143-9474-10
Package Description:
10 VIAL in 1 PACKAGE / 1280 mg in 1 VIAL (0143-9474-01)
Product Code:
0143-9474
Proprietary Name:
Vancomycin Hydrochloride
Non-Proprietary Name:
Vancomycin Hydrochloride
Substance Name:
Vancomycin Hydrochloride
Usage Information:
Vancomycin Hydrochloride for Injection administered intravenously is indicated in adults and pediatric patients less than 18 years of age for the treatment of septicemia due to:Susceptible isolates of methicillin-resistant Staphylococcus aureus (MRSA) and coagulase negative staphylococci.Methicillin-susceptible staphylococci in penicillin-allergic patients, or those patients who cannot receive or who have failed to respond to other drugs, including penicillins or cephalosporins.
11-Digit NDC Billing Format:
00143947410
NDC to RxNorm Crosswalk:
Product Type:
Human Prescription Drug
Labeler Name:
Hikma Pharmaceuticals Usa Inc.
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.
  • Oral - Administration to or by way of the mouth.
Active Ingredient(s):
VANCOMYCIN HYDROCHLORIDE 1280 mg/mg
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
NDA210274
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
08-13-2025
Listing Expiration Date:
12-31-2026
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 0143-9474-10?

The NDC Packaged Code 0143-9474-10 is assigned to a package of 10 vial in 1 package / 1280 mg in 1 vial (0143-9474-01) of Vancomycin Hydrochloride, a human prescription drug labeled by Hikma Pharmaceuticals Usa Inc.. The product's dosage form is injection, powder, for solution and is administered via intravenous; oral form.

Is NDC 0143-9474 included in the NDC Directory?

Yes, Vancomycin Hydrochloride with product code 0143-9474 is active and included in the NDC Directory. The product was first marketed by Hikma Pharmaceuticals Usa Inc. on August 13, 2025 and its listing in the NDC Directory is set to expire on December 31, 2026 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 0143-9474-10?

The 11-digit format is 00143947410. 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
4-4-20143-9474-105-4-200143-9474-10