Oxaliplatin Injection, Solution
NDC Package 42677-337-10

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

Package Information

Oxaliplatin injection is a medication used to treat advanced cancer of the colon and rectum. This formulation utilizes a injection, solution delivery system. Marketed by Shandong New Time Pharmaceutical Co., Ltd., this product is identified by NDC 42677-337 and is authorized under FDA application ANDA219765.

Identification & Billing

NDC Package Code
42677-337-10
Package Description
10 VIAL, SINGLE-DOSE in 1 CARTON / 20 mL in 1 VIAL, SINGLE-DOSE (42677-337-01)
Product Code
42677-337
11-Digit Billing Format
42677033710
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Oxaliplatin
Non-Proprietary Name
Oxaliplatin
Substance Name
Oxaliplatin
Dosage Form
Injection, Solution - A liquid preparation containing one or more drug substances dissolved in a suitable solvent or mixture of mutually miscible solvents that is suitable for injection.
Administration Route
Intravenous - Administration within or into a vein or veins.
Active Ingredient(s)
OXALIPLATIN 5 mg/mL
Pharmacologic Class
Usage Information
This medication is used to treat advanced cancer of the colon and rectum. Oxaliplatin is a chemotherapy drug that contains platinum. It is used to slow or stop cancer cell growth.

Regulatory & Marketing

Labeler Name
Shandong New Time Pharmaceutical Co., Ltd.
Product Type
Human Prescription Drug
FDA Application #
ANDA219765
Marketing Category
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date
01-15-2026
Listing Expiration
12-31-2027
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 42677-337-10 identifies a specific commercial package of 10 vial, single-dose in 1 carton / 20 ml in 1 vial, single-dose (42677-337-01) of Oxaliplatin, a human prescription drug labeled by Shandong New Time Pharmaceutical Co., Ltd.. This injection, solution is formulated for intravenous use and contains oxaliplatin 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 Shandong New Time Pharmaceutical Co., Ltd. on January 15, 2026. The current certification is valid through December 31, 2027.

What are the primary indications for this medication?

This medication is used to treat advanced cancer of the colon and rectum. Oxaliplatin is a chemotherapy drug that contains platinum. It is used to slow or stop cancer cell growth.

How is this Shandong New Time Pharmaceutical Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 42677033710. 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)
42677-337-10
11-Digit CMS (5-4-2)
42677-0337-10

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