XPRO America offers expert assistance for USFDA NDC (National Drug Code) Registration, required for companies manufacturing, repacking, relabeling, or distributing drug products in the United States.

The process involves detailed submission of product and label information in compliance with FDA regulations. Our team streamlines this process, ensuring accurate registration and faster approval.

Our Services Include:

·       Assistance with NDC Code application and registration

·       Guidance on FDA labeling and compliance requirements

·       Review and submission of product details to FDA

· End-to-end support until NDC code is issued

Ideal for pharmaceutical manufacturers, distributors, and exporters selling in the U.S. market.