NDC11 51991007405
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 |
|---|---|
| 51991-0074-05 | 51991-0074 |
| 51991-0074-5 | 51991-0074 |
| 51991-074-05 | 51991-074 |
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 |
|---|---|---|---|---|---|---|
| Ascomp with Codeine | BUTALBITAL, ASPIRIN, CAFFEINE AND CODEINE PHOSPHATE | Breckenridge Pharmaceutical, Inc. | 243a6aea-0f48-42a9-a85e-ff247ab94336 | 2026-02-09 | Boxed warning, Warnings, Adverse reactions | 51991-074-05 51991-074 51991007405 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.