NDC11 78206012901
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 |
|---|---|
| 78206-0129-01 | 78206-0129 |
| 78206-0129-1 | 78206-0129 |
| 78206-129-01 | 78206-129 |
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 |
|---|---|---|---|---|---|---|
| Follistim AQ | FOLLITROPIN | Organon LLC | 48489027-e52b-4b10-ae74-4ba03839150c | 2026-05-26 | Warnings, Adverse reactions | 78206-129-01 78206-129 78206012901 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.