NDC11 43066009025
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 |
|---|---|
| 43066-0090-25 | 43066-0090 |
| 43066-090-25 | 43066-090 |
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 | Baxter Healthcare Corporation | 11cb37c7-01b4-4223-b2ea-a3695639b80b | 2021-04-26 | Boxed warning, Warnings, Adverse reactions | 43066-090-25 43066-090 43066009025 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.