NDC11 69367027216
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 |
|---|---|
| 69367-0272-16 | 69367-0272 |
| 69367-272-16 | 69367-272 |
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 |
|---|---|---|---|---|---|---|
| Codeine-Guaifenesin | CODEINE PHOSPHATE AND GUAIFENESIN | Westminster Pharmaceuticals, LLC | 3da3efd7-e278-4d79-9130-eef3992097e4 | 2025-05-08 | Warnings | 69367-272-16 69367-272 69367027216 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.