NDC11 70700027205
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 |
|---|---|
| 70700-0272-05 | 70700-0272 |
| 70700-0272-5 | 70700-0272 |
| 70700-272-05 | 70700-272 |
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 |
|---|---|---|---|---|---|---|
| Ramelteon | RAMELTEON | Xiromed, LLC | 5c1ba52a-8e7a-844a-6c48-d1c9bf9fff0e | 2022-08-02 | Warnings, Adverse reactions | 70700-272-05 70700-272 70700027205 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.