NDC11 69918073110
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 |
|---|---|
| 69918-0731-10 | 69918-0731 |
| 69918-731-10 | 69918-731 |
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 |
|---|---|---|---|---|---|---|
| Isoproterenol Hydrochloride | ISOPROTERENOL HYDROCHLORIDE | Nordic Pharma, Inc. | 046f2941-3bc0-4755-861c-71bedb49e706 | 2024-06-27 | Warnings, Adverse reactions | 69918-731-10 69918-731 69918073110 |
| Isoproterenol Hydrochloride | ISOPROTERENOL HYDROCHLORIDE | Nordic Pharma, Inc. | 124f44db-b6ba-4886-bfc7-8c71e60ac5b4 | 2024-06-20 | Warnings, Adverse reactions | 69918-731 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.