NDC11 76420089130
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 |
|---|---|
| 76420-0891-30 | 76420-0891 |
| 76420-891-30 | 76420-891 |
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 |
|---|---|---|---|---|---|---|
| Ibuprofen and famotidine | IBUPROFEN AND FAMOTIDINE | Asclemed USA, Inc. | 41123df3-97ac-4c4f-9a89-f76ec03898bb | 2025-01-02 | Boxed warning, Warnings, Adverse reactions | 76420-891-30 76420-891 76420089130 |