NDC11 70069066110
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 |
|---|---|
| 70069-0661-10 | 70069-0661 |
| 70069-661-10 | 70069-661 |
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 |
|---|---|---|---|---|---|---|
| Nalbuphine hydrochloride | NALBUPHINE HYDROCHLORIDE | Somerset Therapeutics, LLC | d82dafac-cce7-445a-8127-2a10b6d947ca | 2024-09-26 | Boxed warning, Adverse reactions | 70069-661-10 70069-661 70069066110 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.