NDC11 00115992201
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 |
|---|---|
| 00115-9922-01 | 00115-9922 |
| 00115-9922-1 | 00115-9922 |
| 0115-9922-01 | 0115-9922 |
Observed NDC auxiliary status history#
This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
| Captured / source date | Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Archive | Snapshot | Source SHA-256 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2020-12-18 03:04 UTC · source 2020-12-17 | excluded package | package | 0115-9922 | 0115-9922-01 | I | Inactivated by FDA | excluded / ndc_excluded.zip | e2bbac7714bc… | 27bdfed8d636… |
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 |
|---|---|---|---|---|---|---|
| Dexmethylphenidate hydrochloride | DEXMETHYLPHENIDATE HYDROCHLORIDE | Amneal Pharmaceuticals of New York LLC | 93e56455-0f15-4ed9-a63a-7fbd0697d520 | 2025-10-09 | Boxed warning, Warnings, Adverse reactions | 0115-9922-01 0115-9922 00115992201 |