NDC11 70839036204
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 |
|---|---|
| 70839-0362-04 | 70839-0362 |
| 70839-0362-4 | 70839-0362 |
| 70839-362-04 | 70839-362 |
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 |
|---|---|---|---|---|---|---|
| COCAINE HYDROCHLORIDE | COCAINE HYDROCHLORIDE | LXO US INC. | 0fb0298f-9756-26e8-e063-6294a90ae8f2 | 2024-01-25 | Boxed warning, Warnings, Adverse reactions | 70839-362-04 70839-362 70839036204 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.