Navinta LLC has applied to the Drug Enforcement Administration to become a registered bulk manufacturer of certain controlled substances. This registration is part of the process to gain approval for manufacturing these substances for validation purposes, which is a step required by the Food Administration before the substances can be distributed to their customers. The public, including current manufacturers of these substances, can submit comments or objections electronically by February 4, 2025. Comments should be submitted through the Federal eRulemaking Portal to ensure they are properly received.
Simple Explanation
Navinta LLC wants to make special kinds of medicines and needs permission first. People have a chance to say if they think this is okay or not by February 4, 2025.