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  5. NDC Package Code: 70069-836-01 Bortezomib

NDC Package 70069-836-01 Bortezomib

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

Table of Contents

    1. Package Information
    2. NDC HCPCS Crosswalk
    3. 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:
70069-836-01
Package Description:
1 VIAL in 1 CARTON / 3.5 mL in 1 VIAL
Product Code:
70069-836
Proprietary Name:
Bortezomib
Non-Proprietary Name:
Bortezomib
Substance Name:
Bortezomib
Usage Information:
This medication is used to treat certain types of cancer (such as multiple myeloma, mantle cell lymphoma). It works by slowing or stopping the growth of cancer cells.
11-Digit NDC Billing Format:
70069083601
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
1 EA
NDC to RxNorm Crosswalk:
RxCUI: 402243 - bortezomib 3.5 MG Injection
Product Type:
Human Prescription Drug
Labeler Name:
Somerset Therapeutics Llc
Dosage Form:
Injection, Powder, Lyophilized, For Solution - A dosage form intended for the solution prepared by lyophilization ("freeze drying"), a process which involves the removal of water from products in the frozen state at extremely low pressures; this is intended for subsequent addition of liquid to create a solution that conforms in all respects to the requirements for Injections.
Administration Route(s):
  • Intravenous - Administration within or into a vein or veins.
  • Subcutaneous - Administration beneath the skin; hypodermic. Synonymous with the term SUBDERMAL.
Active Ingredient(s):
BORTEZOMIB 3.5 mg/3.5mL
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
ANDA211898
Marketing Category:
ANDA - A product marketed under an approved Abbreviated New Drug Application.
Start Marketing Date:
04-29-2025
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.

NDC HCPCS Crosswalk

This crosswalk is intended to help the public understand which drug products (identified by NDCs) are assigned to which HCPCS billing codes.

NDC 70069-836-01 HCPCS crosswalk information with package details and bill units information.

NDC Billing CodeHCPCS CodeHCPCS Code Desc.DosagePackage SizePackage QuantityBillable UnitsBillable Units / Pkg
70069083601J9041INJECTION, BORTEZOMIB, 0.1 MG0.1 MG1EA

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 70069-836-01?

The NDC Packaged Code 70069-836-01 is assigned to a package of 1 vial in 1 carton / 3.5 ml in 1 vial of Bortezomib, a human prescription drug labeled by Somerset Therapeutics Llc. The product's dosage form is injection, powder, lyophilized, for solution and is administered via intravenous; subcutaneous form.This product is billed for "EA" each discreet unit and contains an estimated amount of 1 billable units per package.

Is NDC 70069-836 included in the NDC Directory?

Yes, Bortezomib with product code 70069-836 is active and included in the NDC Directory. The product was first marketed by Somerset Therapeutics Llc on April 29, 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 NDC billing unit for package 70069-836-01?

The contents of this package are billed per "each", products billed on a per each basis are usually products dispensed in discreet units. The calculated billable units for this package is 1.

What is the 11-digit format for NDC 70069-836-01?

The 11-digit format is 70069083601. 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 5-3-2 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
5-3-270069-836-015-4-270069-0836-01