NDC 69336-802-02 - Silivex
This NDC is not currently matched to an FDA NDC product listing in FDA.report, but it is a valid NDC-form code. FDA.report is showing the available DailyMed label context for the product root.
- Product NDC
- 69336-802
- Requested NDC
- 69336-802-02
- Package NDCs from labels
- 69336-802-04, 69336-802-02
- Manufacturer
- Sterling-Knight Pharmaceuticals, LLC
- Effective date
- 2018-09-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Silivex - Sterling-Knight Pharmaceuticals, LLC | Sterling-Knight Pharmaceuticals, LLC | 2018-09-19 | MEDICAL DEVICE |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 69336-802-04 | EA - Each | 69336-802 | ce6fe539-b2f9-4bab-8b75-77ae71fbacc4 | 1 | 2018-08-13 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.