NDC11 00113014190
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 |
|---|---|
| 00113-0141-90 | 00113-0141 |
| 00113-141-90 | 00113-141 |
| 0113-0141-90 | 0113-0141 |
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 |
|---|---|---|---|---|---|---|
| good sense acid reducer | FAMOTIDINE | L. Perrigo Company | cc77f6ff-a534-4731-b971-491280840899 | 2026-05-18 | Warnings | 0113-0141-90 0113-0141 00113014190 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.