NDC11 70069075210
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 |
|---|---|
| 70069-0752-10 | 70069-0752 |
| 70069-752-10 | 70069-752 |
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 |
|---|---|---|---|---|---|---|
| Bupivacaine hydrochloride | BUPIVACAINE HYDROCHLORIDE | Somerset Therapeutics, LLC | bcaab86f-20f0-4482-8d73-e29b36dced58 | 2024-06-20 | Boxed warning, Warnings, Adverse reactions | 70069-752-10 70069-752 70069075210 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.