Vancomycin Hydrochloride Injection, Powder, For Solution
NDC Package 71467-014-01

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Vancomycin Hydrochloride injection is classified as a

administered via intravenous; oral route. This formulation utilizes a injection, powder, for solution delivery system. Marketed by Zhejiang Novus Pharma Co., Ltd., this product is identified by NDC 71467-014 and is authorized under FDA application NDA210274.

Identification & Billing

NDC Package Code
71467-014-01
Package Description
1 VIAL, PHARMACY BULK PACKAGE in 1 CARTON / 10.25 g in 1 VIAL, PHARMACY BULK PACKAGE
Product Code
71467-014
11-Digit Billing Format
71467001401

Clinical Specifications

Proprietary Name
Vancomycin Hydrochloride
Non-Proprietary Name
Vancomycin Hydrochloride
Substance Name
Vancomycin Hydrochloride
Dosage Form
Injection, Powder, For Solution - A sterile preparation intended for reconstitution to form a solution for parenteral use.
Administration Route
  • Intravenous - Administration within or into a vein or veins.
  • Oral - Administration to or by way of the mouth.
Active Ingredient(s)
VANCOMYCIN HYDROCHLORIDE 10.25 g/g
Pharmacologic Class

Regulatory & Marketing

Labeler Name
Zhejiang Novus Pharma Co., Ltd.
Product Type
Human Prescription Drug
FDA Application #
NDA210274
Marketing Category
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date
08-23-2024
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 71467-014-01 identifies a specific commercial package of 1 vial, pharmacy bulk package in 1 carton / 10.25 g in 1 vial, pharmacy bulk package of Vancomycin Hydrochloride, a human prescription drug labeled by Zhejiang Novus Pharma Co., Ltd.. This injection, powder, for solution is formulated for intravenous; oral use and contains vancomycin hydrochloride as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Zhejiang Novus Pharma Co., Ltd. on August 23, 2024. The current certification is valid through December 31, 2026.

How is this Zhejiang Novus Pharma Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 71467001401. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
71467-014-01
11-Digit CMS (5-4-2)
71467-0014-01

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.