Form DHHS 227 is used by businesses and institutions in North Carolina to apply for reregistration under the Controlled Substances Act of 1971. Any entity that manufactures, distributes, researches, or handles controlled substances must complete this form to keep its state authorization active.
Businesses that must file the 227 form include manufacturers, distributors, wholesale distributors, importers and exporters, dispensers, analytical laboratories, researchers, and dog handlers. Each business category has its own registration fee and applies to specific drug schedules. Applicants must also list all drug code numbers relevant to their operations on the form.
The form requires applicants to declare their authorization under both state and federal law. Any prior legal infractions that might affect eligibility must be disclosed. If a previous registration was denied or revoked, the applicant must attach a written explanation. The completed form and payment are mailed to the NC DHHS Controller's Office.
If you work with controlled substances in North Carolina, you may also need related compliance forms. Review the DHHS 2089 form, the DHHS 2124 form, and the DHHS incident report for additional requirements. Facilities that track medications should also keep a controlled drug log.
| Question | Answer |
|---|---|
| Form Name | 227 Form |
| Form Length | 1 pages |
| Fillable? | No |
| Fillable fields | 0 |
| Avg. time to fill out | 15 sec |
| Other names | 227 form printable, 227 form print, 227 reregistration form, 227 form pdf |
