NDC Package 21695-644-10 Altabax

View Billable Units, 11-Digit Format, RxNorm

Package Information
Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

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:

21695-644-10

Package Description:

10 g in 1 TUBE

Product Code:

21695-644

Proprietary Name:

Altabax

Usage Information:

ALTABAX is indicated for use in adults and pediatric patients aged 9 months and older for the topical treatment of impetigo (up to 100 cm2 in total area in adults or 2% total body surface area in pediatric patients aged 9 months or older) due to Staphylococcus aureus (methicillin-susceptible isolates only) or Streptococcus pyogenes[see Clinical Studies (14)].To reduce the development of drug-resistant bacteria and maintain the effectiveness of ALTABAX and other antibacterial drugs, ALTABAX should

11-Digit NDC Billing Format:

21695064410

Billing Unit:

GM - Billing unit of "gram" is used when a product is measured by its weight.

NDC to RxNorm Crosswalk:

10 GM

NDC to RxNorm Crosswalk:

RxCUI: 704855 - retapamulin 1 % Topical Ointment

RxCUI: 704855 - retapamulin 0.01 MG/MG Topical Ointment

RxCUI: 704858 - ALTABAX 1 % Topical Ointment

RxCUI: 704858 - retapamulin 0.01 MG/MG Topical Ointment [Altabax]

RxCUI: 704858 - Altabax 0.01 MG/MG Topical Ointment

Labeler Name:

Rebel Distributors Corp.

Sample Package:

Start Marketing Date:

01-07-2010

Listing Expiration Date:

12-31-2017

Exclude Flag:

Code Structure:

21695 - Rebel Distributors Corp.
- 21695-644 - Altabax
  - 21695-644-10 - 10 g in 1 TUBE

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 21695-644-10?

The NDC Packaged Code 21695-644-10 is assigned to a package of 10 g in 1 tube of Altabax, labeled by Rebel Distributors Corp.. The product's dosage form is and is administered via form.This product is billed per "GM" gram and contains an estimated amount of 10 billable units per package.

Is NDC 21695-644 included in the NDC Directory?

No, Altabax with product code 21695-644 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by Rebel Distributors Corp. on January 07, 2010 and its listing in the NDC Directory is set to expire on December 31, 2017 if the product is not updated or renewed by the manufacturer.

What is the NDC billing unit for package 21695-644-10?

The contents of this package are billed per "gm or gram", products billed per gram are products measured by weight. The calculated billable units for this package is 10.

What is the 11-digit format for NDC 21695-644-10?

The 11-digit format is 21695064410. 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 Format	10-Digit Original Code	11-Digit Format	11-Digit Code
5-3-2	21695-644-10	5-4-2	21695-0644-10

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