NDC Package 16110-518-30 Altabax

View Billable Units, 11-Digit Format, RxNorm

Package Information
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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:

16110-518-30

Package Description:

1 TUBE in 1 CARTON / 30 g in 1 TUBE

Product Code:

16110-518

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)]. Safety in patients younger than 9 months has not been established.To reduce the development of drug resistant bacteria and maintain the effectiveness of ALTABAX and other antibacterial drugs, ALTABAX should be used only to treat or prevent infections that are proven or strongly suspected to be caused by susceptible bacteria.

11-Digit NDC Billing Format:

16110051830

Labeler Name:

Almirall, Llc

Sample Package:

FDA Application Number:

NDA022055

Marketing Category:

NDA - A product marketed under an approved New Drug Application.

Start Marketing Date:

05-01-2016

End Marketing Date:

03-01-2024

Listing Expiration Date:

03-01-2024

Exclude Flag:

Code Structure:

16110 - Almirall, Llc
- 16110-518 - Altabax
  - 16110-518-30 - 1 TUBE in 1 CARTON / 30 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.

Other Product Packages

The following packages are also available for this product:

NDC Package Code	Package Description
16110-518-15	1 TUBE in 1 CARTON / 15 g in 1 TUBE

* Please review the disclaimer below.

Frequently Asked Questions

What is NDC 16110-518-30?

The NDC Packaged Code 16110-518-30 is assigned to a package of 1 tube in 1 carton / 30 g in 1 tube of Altabax, labeled by Almirall, Llc. The product's dosage form is and is administered via form.

Is NDC 16110-518 included in the NDC Directory?

No, Altabax with product code 16110-518 is excluded from the NDC Directory because it was discontinued by the manufacturer. The product was first marketed by Almirall, Llc on May 01, 2016 and its listing in the NDC Directory is set to expire on March 01, 2024 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 16110-518-30?

The 11-digit format is 16110051830. 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	16110-518-30	5-4-2	16110-0518-30

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