NDC11 71839014310
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 |
|---|---|
| 71839-0143-10 | 71839-0143 |
| 71839-143-10 | 71839-143 |
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 |
|---|---|---|---|---|---|---|
| Norepinephrine Bitartrate | NOREPINEPHRINE BITARTRATE | BE Pharmaceuticals Inc. | c42d425a-094e-4390-b4f9-4bb4b0fbc7d0 | 2023-12-30 | Warnings, Adverse reactions | 71839-143-10 71839-143 71839014310 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.