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  5. NDC Package Code: 70710-2091-3 Beizray

NDC Package 70710-2091-3 Beizray

Docetaxel Kit - 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:
70710-2091-3
Package Description:
1 KIT in 1 KIT * 4 mL in 1 VIAL, GLASS (70710-2090-1) * 50 mL in 1 VIAL, GLASS (64208-2512-4)
Product Code:
70710-2091
Proprietary Name:
Beizray
Non-Proprietary Name:
Docetaxel
Usage Information:
This medication is used to treat cancer (such as breast, lung, prostate, stomach, and head/neck cancer). Docetaxel is a member of a family of drugs called taxanes. This drug works by slowing cell growth.
11-Digit NDC Billing Format:
70710209103
Product Type:
Human Prescription Drug
Labeler Name:
Zydus Pharmaceuticals Usa Inc.
Dosage Form:
Kit - A packaged collection of related material.
Sample Package:
No
FDA Application Number:
NDA218711
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
08-28-2025
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 70710-2091-3?

The NDC Packaged Code 70710-2091-3 is assigned to a package of 1 kit in 1 kit * 4 ml in 1 vial, glass (70710-2090-1) * 50 ml in 1 vial, glass (64208-2512-4) of Beizray, a human prescription drug labeled by Zydus Pharmaceuticals Usa Inc.. The product's dosage form is kit and is administered via form.

Is NDC 70710-2091 included in the NDC Directory?

Yes, Beizray with product code 70710-2091 is active and included in the NDC Directory. The product was first marketed by Zydus Pharmaceuticals Usa Inc. on August 28, 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 70710-2091-3?

The 11-digit format is 70710209103. 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 5-4-1 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
5-4-170710-2091-35-4-270710-2091-03