NDC11 49580084208
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 |
|---|---|
| 49580-0842-08 | 49580-0842 |
| 49580-0842-8 | 49580-0842 |
| 49580-842-08 | 49580-842 |
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 |
|---|---|---|---|---|---|---|
| Stomach Relief Ultra Strength | BISMUTH SUBSALICYLATE | P & L Development, LLC | cb5ca7ab-39cf-4b07-ac22-a00b214db102 | 2024-04-16 | Warnings | 49580-0842-8 49580-0842 49580084208 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.