NDC11 64850062205
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 |
|---|---|
| 64850-0622-05 | 64850-0622 |
| 64850-0622-5 | 64850-0622 |
| 64850-622-05 | 64850-622 |
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 |
|---|---|---|---|---|---|---|
| Oxycodone Hydrochloride and Acetaminophen | OXYCODONE HYDROCHLORIDE AND ACETAMINOPHEN | Elite Laboratories, Inc. | 27fa8190-d334-4bb9-b277-d1f44db433e3 | 2026-04-09 | Boxed warning, Warnings, Adverse reactions | 64850-622-05 64850-622 64850062205 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.