NDC11 47335089419
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 |
|---|---|
| 47335-0894-19 | 47335-0894 |
| 47335-894-19 | 47335-894 |
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 |
|---|---|---|---|---|---|---|
| Clopidogrel Bisulfate | CLOPIDOGREL BISULFATE | Sun Pharmaceutical Industries, Inc. | d37db064-3a5a-4a0c-a60b-b4b417fe742a | 2022-09-23 | Boxed warning, Warnings, Adverse reactions | 47335-894-19 47335-894 47335089419 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.