NDC11 72288075600
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 |
|---|---|
| 72288-0756-0 | 72288-0756 |
| 72288-0756-00 | 72288-0756 |
| 72288-756-00 | 72288-756 |
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 | Amazon.com Services LLC | d5823283-aa97-451e-ba0d-69f0e79c8514 | 2026-08-31 | Warnings | 72288-756-00 72288-756 72288075600 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.