NDC11 83205000102
This exact 11-digit normalized identifier can correspond to more than one FDA hyphenation. FDA.report preserves the exact identifier and exposes every structurally valid candidate without guessing.
Possible FDA NDC forms#
| Package NDC | Product root |
|---|---|
| 83205-0001-02 | 83205-0001 |
| 83205-0001-2 | 83205-0001 |
| 83205-001-02 | 83205-001 |
openFDA label cross-check#
OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
| Brand | Generic | Manufacturer | SPL set ID | Effective date | Available safety fields | Join |
|---|---|---|---|---|---|---|
| TECELRA | AFAMITRESGENE AUTOLEUCEL | USWM CT, LLC | ab24631f-3364-46e1-8074-7244863bcbab | 2026-07-15 | Boxed warning, Warnings, Adverse reactions | 83205-0001-2 83205-0001 83205000102 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.