NDC11 00135058201
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 |
|---|---|
| 00135-0582-01 | 00135-0582 |
| 00135-0582-1 | 00135-0582 |
| 00135-582-01 | 00135-582 |
| 0135-0582-01 | 0135-0582 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2020-06-10 20:45 UTC · source 2020-06-10 | excluded package | package | 0135-0582 | 0135-0582-01 | I | Inactivated by FDA | excluded / ndc_excluded.zip | 9bebd1f3094a… | 5416666fcb17… |
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 |
|---|---|---|---|---|---|---|
| CHILDRENS FLONASE ALLERGY RELIEF | FLUTICASONE PROPIONATE | Haleon US Holdings LLC | fab7a1f4-75e0-416f-9644-07aff08e6ab0 | 2024-03-05 | Warnings | 0135-0582 |
| CHILDRENS FLONASE ALLERGY RELIEF | FLUTICASONE PROPIONATE | Haleon US Holdings LLC | 3adff80f-fca7-4cc5-b106-0f68f71c85b0 | 2024-02-08 | Warnings | 0135-0582-01 0135-0582 00135058201 |