NDC11 73352090501
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 |
|---|---|
| 73352-0905-01 | 73352-0905 |
| 73352-0905-1 | 73352-0905 |
| 73352-905-01 | 73352-905 |
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 |
|---|---|---|---|---|---|---|
| Lactulose | LACTULOSE | Trifluent Pharma, Inc. | 3eaf273a-b49d-2595-e063-6394a90a1cf6 | 2025-09-13 | Warnings, Adverse reactions | 73352-905-01 73352-905 73352090501 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.