NDC11 42507019471
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 |
|---|---|
| 42507-0194-71 | 42507-0194 |
| 42507-194-71 | 42507-194 |
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 |
|---|---|---|---|---|---|---|
| ACID REDUCER | FAMOTIDINE | HyVee Inc | 381db08e-5756-4255-8202-1d8e6a1cf038 | 2026-06-03 | Warnings | 42507-194-71 42507-194 42507019471 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.