NDC11 51991098317
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 |
|---|---|
| 51991-0983-17 | 51991-0983 |
| 51991-983-17 | 51991-983 |
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 | Breckenridge Pharmaceutical, Inc. | 109aa5e6-4e42-4131-97b0-f24d3a4cb4e8 | 2026-08-27 | Warnings, Adverse reactions | 51991-983-17 51991-983 51991098317 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.