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Electronic Drug Listing and Registration Guides

Aug 6, 2020 | Drug & Biologic Product Submissions, Pharmaceutical and Cosmetics

To learn the main requirements for Electronic Drug Registration and Labeling (eDRL), download a quick-reference guide with step-by-step instructions and ways to simplify and expedite the process. Download your free guide here.

The eDRL How-to Guide answers questions like:

  • Who is responsible to list a drug product?
  • How to obtain Drug Listing and National Drug Codes (NDCs)?
  • What are the prerequisites for drug listing submissions?
  • What are the elements of a drug listing submission?
  • What are the manufacturer’s listing and enforcement issues?

We hope you find this reference information as a helpful resource to your team. If you have questions about Drug Listings for OTC, prescription or other scenarios, contact us. We are here to help. Email: [email protected]