NDC11 75568003701
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 |
|---|---|
| 75568-0037-01 | 75568-0037 |
| 75568-0037-1 | 75568-0037 |
| 75568-037-01 | 75568-037 |
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 |
|---|---|---|---|---|---|---|
| Orythia Maximum Strength Lidocaine Pain Relieving | LIDOCAINE | Planet (Anhui) Pharmaceutical Co., Ltd. | 6d6b59f9-f614-4e3c-b07b-32b4591d39f2 | 2025-08-18 | Warnings | 75568-037-01 75568-037 75568003701 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.