NDC11 00338010820
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 |
|---|---|
| 00338-0108-20 | 00338-0108 |
| 00338-108-20 | 00338-108 |
| 0338-0108-20 | 0338-0108 |
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 | Baxter Healthcare Corporation | 6363e9b4-29df-4553-904d-a563e5adda6e | 2026-02-06 | Warnings, Adverse reactions | 0338-0108-20 0338-0108 00338010820 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.