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  5. NDC Package Code: 24338-340-05 Gleostine

NDC Package 24338-340-05 Gleostine

Lomustine Capsule, Gelatin Coated 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:
24338-340-05
Package Description:
1 BOTTLE in 1 CARTON / 5 CAPSULE, GELATIN COATED in 1 BOTTLE
Product Code:
24338-340
Proprietary Name:
Gleostine
Non-Proprietary Name:
Lomustine
Substance Name:
Lomustine
Usage Information:
This medication is used to treat various types of cancer. Lomustine belongs to a class of drugs known as alkylating agents. It works by slowing or stopping the growth of cancer cells.
11-Digit NDC Billing Format:
24338034005
Product Type:
Human Prescription Drug
Labeler Name:
Azurity Pharmaceuticals, Inc.
Dosage Form:
Capsule, Gelatin Coated - A solid dosage form in which the drug is enclosed within either a hard or soft soluble container made from a suitable form of gelatin; through a banding process, the capsule is coated with additional layers of gelatin so as to form a complete seal.
Administration Route(s):
Oral - Administration to or by way of the mouth.
Active Ingredient(s):
LOMUSTINE 10 mg/1
Pharmacologic Class(es):
Sample Package:
No
FDA Application Number:
NDA017588
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
10-24-2025
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 24338-340-05?

The NDC Packaged Code 24338-340-05 is assigned to a package of 1 bottle in 1 carton / 5 capsule, gelatin coated in 1 bottle of Gleostine, a human prescription drug labeled by Azurity Pharmaceuticals, Inc.. The product's dosage form is capsule, gelatin coated and is administered via oral form.

Is NDC 24338-340 included in the NDC Directory?

Yes, Gleostine with product code 24338-340 is active and included in the NDC Directory. The product was first marketed by Azurity Pharmaceuticals, Inc. on October 24, 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 24338-340-05?

The 11-digit format is 24338034005. 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
5-3-224338-340-055-4-224338-0340-05