NDC11 68180099706
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 |
|---|---|
| 68180-0997-06 | 68180-0997 |
| 68180-0997-6 | 68180-0997 |
| 68180-997-06 | 68180-997 |
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 |
|---|---|---|---|---|---|---|
| Fluoxetine Hydrochloride | FLUOXETINE HYDROCHLORIDE | Lupin Pharmaceuticals, Inc. | f274f102-67ec-46e7-b248-533be2e3003b | 2025-03-06 | Boxed warning, Warnings, Adverse reactions | 68180-997-06 68180-997 68180099706 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.