NDC11 71981002007
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 |
|---|---|
| 71981-0020-07 | 71981-0020 |
| 71981-0020-7 | 71981-0020 |
| 71981-020-07 | 71981-020 |
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 |
|---|---|---|---|---|---|---|
| OXERVATE | CENEGERMIN-BKBJ | Domp farmaceutici S.p.A. | 89e4bfec-d710-40ed-8885-5d13ba46b1cd | 2024-12-31 | Warnings, Adverse reactions | 71981-020-07 71981-020 71981002007 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.