NDC11 41520090172
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 |
|---|---|
| 41520-0901-72 | 41520-0901 |
| 41520-901-72 | 41520-901 |
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 |
|---|---|---|---|---|---|---|
| CareOne Acid Relief | FAMOTIDINE | American Sales Company | ed474c9d-c08b-4f52-8b24-5887978e4275 | 2026-07-01 | Warnings | 41520-901-72 41520-901 41520090172 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.