NDC11 43066099701
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 |
|---|---|
| 43066-0997-01 | 43066-0997 |
| 43066-0997-1 | 43066-0997 |
| 43066-997-01 | 43066-997 |
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 |
|---|---|---|---|---|---|---|
| Norepinephrine Bitartrate | NOREPINEPHRINE BITARTRATE | Baxter Healthcare Company | e375a0b9-4d26-4749-bbc3-43d63a7cf65a | 2021-05-06 | Warnings, Adverse reactions | 43066-997-01 43066-997 43066099701 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.