NDC11 00363014139
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 |
|---|---|
| 00363-0141-39 | 00363-0141 |
| 00363-141-39 | 00363-141 |
| 0363-0141-39 | 0363-0141 |
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 |
|---|---|---|---|---|---|---|
| Acid Controller Original Strength | FAMOTIDINE | Walgreen Company | 98c6ddc9-8103-40b3-a145-ffbe3374ab6c | 2026-03-03 | Warnings | 0363-0141-39 0363-0141 00363014139 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.