NDC11 25021079002
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 |
|---|---|
| 25021-0790-02 | 25021-0790 |
| 25021-0790-2 | 25021-0790 |
| 25021-790-02 | 25021-790 |
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 |
|---|---|---|---|---|---|---|
| PROCHLORPERAZINE EDISYLATE | PROCHLORPERAZINE EDISYLATE | Sagent Pharmaceuticals | fed5ed29-7091-4b3c-bf67-64f32cd189bb | 2022-11-29 | Boxed warning, Warnings, Adverse reactions | 25021-790-02 25021-790 25021079002 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.