NDC11 25021031604
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 |
|---|---|
| 25021-0316-04 | 25021-0316 |
| 25021-0316-4 | 25021-0316 |
| 25021-316-04 | 25021-316 |
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 | Sagent Pharmaceuticals | cc9ecec5-3bd7-4132-9745-7666bac8ceac | 2023-12-31 | Warnings, Adverse reactions | 25021-316-04 25021-316 25021031604 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.