NDC11 72611072201
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 |
|---|---|
| 72611-0722-01 | 72611-0722 |
| 72611-0722-1 | 72611-0722 |
| 72611-722-01 | 72611-722 |
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 |
|---|---|---|---|---|---|---|
| Ketorocaine LM Kit | KETOROLAC TROMETHAMINE, LIDOCAINE HYDROCHLORIDE, BUPIVACAINE HYDROCHLORIDE, POVIDINE IODINE | Advanced Rx Pharmacy of Tennessee, LLC | fb81d452-30e0-f019-e053-6394a90a7634 | 2024-12-31 | Boxed warning, Warnings, Adverse reactions | 72611-722-01 72611072201 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.