Organizations can implement application, database, interface, reporting, labeling, and workflow changes.
The exact timing will depend on internal release cycles and vendor delivery schedules.
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The FDA published the final NDC12 rule on March 5, 2026. The rule takes effect on March 7, 2033, when FDA will begin assigning new 12-digit NDCs and convert existing FDA-assigned 10-digit NDCs to the uniform 12-digit format.
A three-year drug-labeling transition will then continue through March 6, 2036.
FDA begins assigning new NDC12 codes and converts previously assigned FDA NDCs to the 12-digit format.
7 Years
3 Years
12 Digits
6-4-2
| Date | Milestone | Status |
| November 5, 2018 | FDA public hearing on the future NDC format | Completed |
| July 25, 2022 | Proposed NDC format rule published | Completed |
| March 5, 2026 | Final NDC12 rule published | Completed |
| March 5, 2026–March 6, 2033 | Seven-year preparation period | In progress |
| March 7, 2033 | Final rule takes effect | Upcoming |
| March 7, 2033–March 6, 2036 | Drug-labeling transition | Upcoming |
| March 7, 2036 onward | 10-digit NDC labeling may be subject to regulatory action | Upcoming |
FDA discussed the future format of the National Drug Code as the available supply of five-digit labeler codes became limited.
The proposed rule introduced the uniform 12-digit, 6-4-2 structure and requested feedback on format, timing, labeling, barcode requirements, and operational impact.
FDA evaluated stakeholder comments and ultimately selected a seven-year delay between publication and the effective date.
The final rule confirms the 12-digit 6-4-2 format, March 7, 2033 effective date, preparation period, labeling transition, conversion of prior NDC10 codes, and updated barcode provisions.
Understand the three segments used to identify a listed drug
Organizations should establish program ownership and identify where NDCs are created, stored, displayed, converted, printed, scanned, or exchanged. Useful outputs may include:
Understand the three segments used to identify a listed drug
Teams can evaluate how the 12-digit format affects applications, databases, interfaces, labels, reports, and external dependencies.
This phase can also be used to:
Understand the three segments used to identify a listed drug
Organizations can implement application, database, interface, reporting, labeling, and workflow changes.
The exact timing will depend on internal release cycles and vendor delivery schedules.
Understand the three segments used to identify a listed drug
Testing should move beyond individual applications and include connected systems, external files, vendors, scanners, labels, reports, and trading partners.
Understand the three segments used to identify a listed drug
The final period before the effective date should focus on:
Organizations should not treat these checkpoints as universally required dates. They provide a practical way to divide the confirmed seven-year preparation window into manageable phases.
New FDA-assigned NDCs use the uniform 6-4-2 structure.
Previously assigned FDA NDCs are converted by adding leading zeros to the appropriate segments.
FDA plans to automatically update its drug-listing files to reflect the 12-digit format.
Parties using FDA-assigned NDCs need systems capable of handling NDC12 on the effective date.
The three-year period for moving drug labeling from 10 digits to 12 digits begins.
The transition does not delay system readiness. March 7, 2033 remains the system-readiness date; the 2033–2036 period is specifically a labeling transition.
| Workstream | Before March 7, 2033 | March 7, 2033 | Through March 6, 2036 |
|---|---|---|---|
| FDA assignments | Current 10-digit formats continue | New assignments use NDC12 | NDC12 remains the native FDA format |
| Existing NDCs | Existing NDC10 values remain current | FDA converts them to 12 digits | Both representations may remain relevant during transition |
| Systems | Prepare, remediate, and test | Must support | Should support both 10- and 12-digit formats |
| Drug labeling | Prepare revised labeling | NDC12 Label transition begins |
Complete updates and use remaining old stock |
| Drug-listing files | Prepare for format change | FDA automatically updates files | Registrants update listings when labels are updated |
| Historical data | Inventory and plan normalization | Preserve crosswalks and traceability | Continue managing old and new representations |
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