NDC11 48951939605
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 |
|---|---|
| 48951-9396-05 | 48951-9396 |
| 48951-9396-5 | 48951-9396 |
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 |
|---|---|---|---|---|---|---|
| Vespa Crabro DKS | VESPA CRABRO DKS | Uriel Pharmacy Inc. | 06e9e1ff-911f-c048-e063-6394a90ad431 | 2026-08-14 | Warnings | 48951-9396-5 48951-9396 48951939605 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.