NDC11 71205019890
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 |
|---|---|
| 71205-0198-90 | 71205-0198 |
| 71205-198-90 | 71205-198 |
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 |
|---|---|---|---|---|---|---|
| Paroxetine | PAROXETINE HYDROCHLORIDE HEMIHYDRATE | Proficient Rx LP | 903e4ef1-487d-4b65-9038-b05ceaf74d19 | 2024-05-01 | Boxed warning, Warnings, Adverse reactions | 71205-198-90 71205-198 71205019890 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.