NDC11 51672211500
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 |
|---|---|
| 51672-2115-0 | 51672-2115 |
| 51672-2115-00 | 51672-2115 |
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 |
|---|---|---|---|---|---|---|
| Feverall Childrens | ACETAMINOPHEN | Sun Pharmaceutical Industries, Inc. | 861e2987-5473-45b0-b2a6-f980a9b0e809 | 2026-08-24 | Warnings | 51672-2115-0 51672-2115 51672211500 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.