NDC11 51316051163
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 |
|---|---|
| 51316-0511-63 | 51316-0511 |
| 51316-511-63 | 51316-511 |
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 | CVS WOONSOCKET PRESCRIPTION CENTER, INCORPORATED | f347f870-1da4-4a77-8c20-63b703d24071 | 2026-08-05 | Warnings | 51316-511-63 51316-511 51316051163 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.