Dotarem Injection
NDC Package 67684-2000-2
Package Information
Dotarem (gadoterate meglumine) injection is dOTAREM is a gadolinium-based contrast agent indicated for intravenous use with magnetic resonance imaging (MRI) in brain (intracranial), spine and associated tissues in adult and pediatric patients (including term neonates) to detect and visualize areas with disruption of the blood brain barrier (BBB) and/or abnormal vascularity. This formulation utilizes a injection delivery system. Marketed by Guerbet Llc, this product is identified by NDC 67684-2000 and is authorized under FDA application NDA204781.
Identification & Billing
Clinical Specifications
- Intravenous - Administration within or into a vein or veins.
- Intravenous - Administration within or into a vein or veins.
Regulatory & Marketing
Hierarchy Structure
- 67684 - Guerbet Llc
- 67684-2000 - Dotarem
- 67684-2000-2 - 10 VIAL in 1 PACKAGE / 15 mL in 1 VIAL
- 67684-2000 - Dotarem
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 (67684-2000). 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 67684-2000-2 identifies a specific commercial package of 10 vial in 1 package / 15 ml in 1 vial of Dotarem, a human prescription drug labeled by Guerbet Llc. This injection is formulated for intravenous use and contains gadoterate meglumine 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 Guerbet Llc on March 20, 2013. The current certification is valid through December 31, 2026.
How is this Guerbet Llc product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 67684200002. 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 Package segment to maintain the 5-4-2 structure.