NDC11 69396011605
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 |
|---|---|
| 69396-0116-05 | 69396-0116 |
| 69396-0116-5 | 69396-0116 |
| 69396-116-05 | 69396-116 |
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 |
|---|---|---|---|---|---|---|
| Saline Ampoules | SODIUM CHLORIDE 0.9% | Trifecta Pharmaceuticals USA, LLC. | ee18ef7c-bb5d-30ec-e053-2a95a90a964e | 2025-10-13 | Warnings | 69396-116-05 69396-116 69396011605 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.