NDC 83559-017
This exact product or package identity exists in FDA auxiliary data but is not present in the current primary NDC product table. The package identity is preserved; status rows are reported source observations, not medical conclusions.
- Requested NDC
- 83559-017
- Product root
- 83559-017
- Identity scope
- Product
- Primary current NDC product row
- Not present
NDC auxiliary status#
These records are reproduced from FDA’s unfinished, excluded, and compounder listings. They describe what appeared in the source files; a missing record does not establish a regulatory status. View all current auxiliary records, including entries without an NDC. · View the auxiliary file history.
| Dataset | Scope | Product NDC | Package NDC | Code | Status | Reporting period | Source date |
|---|---|---|---|---|---|---|---|
| excluded product | product | 83559-017 | E | Excluded after deficient or non-compliant submission was not corrected | 2026-10-02 | ||
| excluded package | package | 83559-017 | 83559-017-01 | E | Excluded after deficient or non-compliant submission was not corrected | 2026-10-02 | |
| excluded package | package | 83559-017 | 83559-017-02 | E | Excluded after deficient or non-compliant submission was not corrected | 2026-10-02 |
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 |
|---|---|---|---|---|---|---|
| ENOKON PAIN RELIEF Cream | PAIN RELIEF CREAM | Henan Enokon Medical Instrument Co., Ltd. | 567502df-d5f0-a3f7-e063-6394a90a57f0 | 2026-07-12 | Warnings | 83559-017 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.