NDC11 83393074908
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 |
|---|---|
| 83393-0749-08 | 83393-0749 |
| 83393-0749-8 | 83393-0749 |
| 83393-749-08 | 83393-749 |
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 |
|---|---|---|---|---|---|---|
| Treda Ultra | BISMUTH SUBSALICYLATE | Laboratorios Sanfer, S.A. de C.V. | cfa7f37a-e18b-4929-b3a4-4126b0aa679a | 2026-02-12 | Warnings | 83393-749-08 83393-749 83393074908 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.