Veltin
NDC Package 16110-071-60

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
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 inactivated by the FDA.

Veltin is ® (clindamycin phosphate and tretinoin) Gel, 1.2%/0.025% is indicated for the topical treatment of acne vulgaris in patients 12 years and older. Marketed by Almirall, Llc, this product is identified by NDC 16110-071 and is authorized under FDA application NDA050803.

Identification & Billing

NDC Package Code
16110-071-60
Package Description
1 TUBE in 1 CARTON / 60 g in 1 TUBE
Product Code
16110-071
11-Digit Billing Format
16110007160
Billing Unit
GM - Billing unit of "gram" is used when a product is measured by its weight.
Units Per Package
60 GM
RxNorm Crosswalk
  • RxCUI: 882548 - clindamycin phosphate 1.2 % / tretinoin 0.025 % Topical Gel
  • RxCUI: 882548 - clindamycin phosphate 0.012 MG/MG / tretinoin 0.00025 MG/MG Topical Gel
  • RxCUI: 882548 - clindamycin phosphate 1.2 % (clindamycin 1 % ) / tretinoin 0.025 % Topical Gel
  • RxCUI: 999927 - VELTIN 1.2 % / 0.025 % Topical Gel
  • RxCUI: 999927 - clindamycin phosphate 0.012 MG/MG / tretinoin 0.00025 MG/MG Topical Gel [Veltin]

Clinical Specifications

Proprietary Name
Veltin
Dosage Form
-
Usage Information
VELTIN® (clindamycin phosphate and tretinoin) Gel, 1.2%/0.025% is indicated for the topical treatment of acne vulgaris in patients 12 years and older.

Regulatory & Marketing

Labeler Name
Almirall, Llc
FDA Application #
NDA050803
Marketing Category
NDA - A product marketed under an approved New Drug Application.
Start Marketing Date
07-29-2010
Listing Expiration
12-31-2023
Exclude Flag
I
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (16110-071). Click a package code to view its specific billing and regulatory data.

16110-071-30
1 TUBE in 1 CARTON / 30 g in 1 TUBE

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 16110-071-60 identifies a specific commercial package of 1 tube in 1 carton / 60 g in 1 tube of Veltin, labeled by Almirall, Llc. This product is billed per "GM" gram and contains an estimated amount of 60 billable units per package. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Almirall, Llc on July 29, 2010. The current certification is valid through December 31, 2023.

How is this Almirall, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 16110007160. Quantities are measured in per "gm or gram", products billed per gram are products measured by weight.. There are 60 total billable units per package. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-3-2)
16110-071-60
11-Digit CMS (5-4-2)
16110-0071-60

Note: The zero is added to the Product segment to maintain the 5-4-2 structure.