NDC11 62135024230
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 |
|---|---|
| 62135-0242-30 | 62135-0242 |
| 62135-242-30 | 62135-242 |
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 |
|---|---|---|---|---|---|---|
| Naltrexone Hydrochloride | NALTREXONE HYDROCHLORIDE | Chartwell RX, LLC | adb7c4dc-221a-4d91-9687-0d78913a92ad | 2026-06-19 | Warnings, Adverse reactions | 62135-242-30 62135-242 62135024230 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.