NDC11 36800090002
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 |
|---|---|
| 36800-0900-02 | 36800-0900 |
| 36800-0900-2 | 36800-0900 |
| 36800-900-02 | 36800-900 |
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 |
|---|---|---|---|---|---|---|
| Pain Relief Regular Strength | ACETAMINOPHEN | TopCo Associates LLC | c2d33352-431c-4683-a4fa-a54437e7b8d2 | 2024-12-02 | Warnings | 36800-900-02 36800-900 36800090002 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.