Zaltrap Solution, Concentrate
NDC Package 0024-5840-03
Package Information
Zaltrap (ziv-aflibercept) solution is ziv-aflibercept is used to treat cancer of the colon and rectum. This formulation utilizes a solution, concentrate delivery system. Marketed by Sanofi-aventis U.s. Llc, this product is identified by NDC 0024-5840 and is authorized under FDA application BLA125418.
Identification & Billing
- RxCUI: 1723187 - ziv-aflibercept 200 MG in 8 ML Injection
- RxCUI: 1723187 - 8 ML ziv-aflibercept 25 MG/ML Injection
- RxCUI: 1723187 - ziv-aflibercept 200 MG per 8 ML Injection
- RxCUI: 1723189 - ZALTRAP 200 MG in 8 ML Injection
- RxCUI: 1723189 - 8 ML ziv-aflibercept 25 MG/ML Injection [Zaltrap]
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 0024 - Sanofi-aventis U.s. Llc
- 0024-5840 - Zaltrap
- 0024-5840-03 - 3 VIAL in 1 CARTON / 4 mL in 1 VIAL
- 0024-5840 - Zaltrap
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 (0024-5840). Click a package code to view its specific billing and regulatory data.
* 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 0024-5840-03 identifies a specific commercial package of 3 vial in 1 carton / 4 ml in 1 vial of Zaltrap, a human prescription drug labeled by Sanofi-aventis U.s. Llc. This solution, concentrate is formulated for intravenous use and contains aflibercept as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Sanofi-aventis U.s. Llc on August 03, 2012. The current certification is valid through December 31, 2026.
What are the primary indications for this medication?
Ziv-aflibercept is used to treat cancer of the colon and rectum.
How is this Sanofi-aventis U.s. Llc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 00024584003. Quantities are measured in per "ml or milliliter", products billed per milliliter are usually products measured by liquid volume.. 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:
Note: The zero is added to the Labeler segment to maintain the 5-4-2 structure.