NDC11 61703030906
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 |
|---|---|
| 61703-0309-06 | 61703-0309 |
| 61703-0309-6 | 61703-0309 |
| 61703-309-06 | 61703-309 |
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 |
|---|---|---|---|---|---|---|
| VinCRIStine Sulfate | VINCRISTINE SULFATE | Hospira, Inc. | b22e4c8e-dbe1-4d4b-a026-e1812974071c | 2026-02-17 | Boxed warning, Warnings, Adverse reactions | 61703-309 |
| VinCRIStine Sulfate | VINCRISTINE SULFATE | Hospira, Inc. | 49596de6-ab18-49d1-9e5b-30968fc21c36 | 2025-12-30 | Boxed warning, Warnings, Adverse reactions | 61703-309-06 61703-309 61703030906 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.