NDC11 72865016801
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 |
|---|---|
| 72865-0168-01 | 72865-0168 |
| 72865-0168-1 | 72865-0168 |
| 72865-168-01 | 72865-168 |
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 |
|---|---|---|---|---|---|---|
| hydromorphone hydrochloride | HYDROMORPHONE HYDROCHLORIDE | XLCare Pharmaceuticals, Inc. | 90bda45c-9dbe-4ed5-91d0-df8446ad7026 | 2024-01-17 | Boxed warning, Warnings, Adverse reactions | 72865-168-01 72865-168 72865016801 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.