NDC11 15631003601
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 |
|---|---|
| 15631-0036-01 | 15631-0036 |
| 15631-0036-1 | 15631-0036 |
| 15631-036-01 | 15631-036 |
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 |
|---|---|---|---|---|---|---|---|---|---|---|
| 2019-12-08 06:16 UTC · source 2019-12-05 | excluded package | package | 15631-0036 | 15631-0036-1 | E | Excluded after deficient or non-compliant submission was not corrected | excluded / ndc_excluded.zip | 110d247fa046… | a55b01930146… |
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 |
|---|---|---|---|---|---|---|
| ANTIMONIUM CRUDUM | ANTIMONIUM CRUDUM | Rxhomeo Private Limited d.b.a. Rxhomeo, Inc | 7e9b478f-1eab-4473-8138-3680dcaa4bfc | 2021-09-27 | Warnings | 15631-0036-1 15631-0036 15631003601 |