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  5. NDC Package Code: 68850-012-02 Myambutol

NDC Package 68850-012-02 Myambutol

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was discontinued by the firm.

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:
68850-012-02
Package Description:
10 BLISTER PACK in 1 BOX, UNIT-DOSE / 10 TABLET, FILM COATED in 1 BLISTER PACK
Product Code:
68850-012
Proprietary Name:
Myambutol
Usage Information:
Ethambutol is used with other medications to treat tuberculosis (TB). Ethambutol is an antibiotic and works by stopping the growth of bacteria. This antibiotic treats only bacterial infections. It will not work for viral infections (such as common cold, flu). Using any antibiotic when it is not needed can cause it to not work for future infections.
11-Digit NDC Billing Format:
68850001202
Billing Unit:
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
NDC to RxNorm Crosswalk:
10 EA
Labeler Name:
Sti Pharma, Llc
Sample Package:
No
FDA Application Number:
NDA016320
Marketing Category:
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date:
08-10-2007
End Marketing Date:
09-30-2024
Listing Expiration Date:
09-30-2024
Exclude Flag:
D
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.

Other Product Packages

The following packages are also available for this product:

NDC Package CodePackage Description
68850-012-01100 TABLET, FILM COATED in 1 BOTTLE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 68850-012-02?

The NDC Packaged Code 68850-012-02 is assigned to a package of 10 blister pack in 1 box, unit-dose / 10 tablet, film coated in 1 blister pack of Myambutol, labeled by Sti Pharma, Llc. The product's dosage form is and is administered via form.

Is NDC 68850-012 included in the NDC Directory?

No, Myambutol with product code 68850-012 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Sti Pharma, Llc on August 10, 2007 and its listing in the NDC Directory is set to expire on September 30, 2024 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 68850-012-02?

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 10.

What is the 11-digit format for NDC 68850-012-02?

The 11-digit format is 68850001202. 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
5-3-268850-012-025-4-268850-0012-02