U.S. FDA Annual Drug Listing Reports

The U.S. Food and Drug Administration (FDA) requires registered Drug Establishments to annually report the distributed quantities for each of their listed drug products. The suggested deadline for reporting drug quantities distributed during calendar year 2022 is February 15, 2023.

Registrar Corp can help file these reports on your behalf as part of our U.S. Agent and Registrant Contact service (Note: Additional fees may apply for migration of listings not currently managed by Registrar Corp). For assistance, simply complete the form below.

U.S. FDA Annual Drug Listing Reports

New Annual Reporting for U.S. FDA Drug Listings

Food for Human Consumption

Food for Animal Consumption

Food for Human Consumption

Food for Animal Consumption

Solutions

About

FDA has cancelled thousands of registrations that were not properly renewed or did not include
an accurate Unique Facility Identifier (UFI). If you need immediate assistance, Registrar Corp can help.

Notice: Medical Device and Drug establishments that did not renew their FDA registrations in must re-register.

FDA-registered facilities must renew their registrations by December 31,

Medical Device and Drug establishments must renew their registrations by December 31,

Reminder

Notice

Limited Time Offer

Manufacturer Name	Registration Number

New Annual Reporting for U.S. FDA Drug Listings

Food for Human Consumption

Food for Animal Consumption

Food for Human Consumption

Food for Animal Consumption

Solutions

About

FDA has cancelled thousands of registrations that were not properly renewed or did not include an accurate Unique Facility Identifier (UFI). If you need immediate assistance, Registrar Corp can help.

Notice: Medical Device and Drug establishments that did not renew their FDA registrations in must re-register.

FDA-registered facilities must renew their registrations by December 31,

Medical Device and Drug establishments must renew their registrations by December 31,

Reminder

Notice

Limited Time Offer

FDA has cancelled thousands of registrations that were not properly renewed or did not include
an accurate Unique Facility Identifier (UFI). If you need immediate assistance, Registrar Corp can help.