NDC Package 66406-0206-3 Tedizolid Phosphate

Tablet, Coated - View Billable Units, 11-Digit Format, RxNorm

Package Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.

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:
66406-0206-3
Package Description:
90 BLISTER PACK in 1 CONTAINER / 1 TABLET, COATED in 1 BLISTER PACK
Product Code:
Non-Proprietary Name:
Tedizolid Phosphate
Substance Name:
Tedizolid Phosphate
Usage Information:
This medication is used to treat serious bacterial infections of the skin. It 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:
66406020603
Product Type:
Drug For Further Processing
Labeler Name:
Patheon Inc.
Dosage Form:
Tablet, Coated - A solid dosage form that contains medicinal substances with or without suitable diluents and is covered with a designated coating.
Active Ingredient(s):
Sample Package:
N/A
Marketing Category:
DRUG FOR FURTHER PROCESSING - A drug (other than the bulk ingredient API) that is in an interim stage of manufacture, processing, preparation, or packaging, and not ready for human or animal use.
Start Marketing Date:
06-20-2014
Listing Expiration Date:
12-31-2024
Exclude Flag:
N
Unfinished Product:
Yes
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
66406-0206-196 BOTTLE in 1 CONTAINER / 30 TABLET, COATED in 1 BOTTLE
66406-0206-290 BLISTER PACK in 1 CONTAINER / 6 TABLET, COATED in 1 BLISTER PACK

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 66406-0206-3?

The NDC Packaged Code 66406-0206-3 is assigned to an UNFINISHED drug package of 90 blister pack in 1 container / 1 tablet, coated in 1 blister pack of Tedizolid Phosphate, drug for further processing labeled by Patheon Inc.. The product's dosage form is tablet, coated and is administered via form.

Is NDC 66406-0206 included in the NDC Directory?

Yes, Tedizolid Phosphate is an UNFINISHED PRODUCT with code 66406-0206 that is active and included in the NDC Directory. The product was first marketed by Patheon Inc. on June 20, 2014 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 66406-0206-3?

The 11-digit format is 66406020603. 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
5-4-166406-0206-35-4-266406-0206-03