NDC 58406-435-01
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
- 58406-435
- Requested NDC
- 58406-435-01
- Package NDCs from labels
- 58406-435-01
- Manufacturer
- National Council for Prescription Drug Programs
- Effective date
- 2012-07-24
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| National Council for Prescription Drug Programs indexing - billing unit | National Council for Prescription Drug Programs | 2012-07-24 | Indexing - Billing Unit |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 58406-435-01 | ML - Milliliter | 58406-435 | 39c8403a-79fd-4323-b6bf-d48311d735d5 | 1 | 2012-07-24 |
| 58406-435-04 | ML - Milliliter | 58406-435 | b3d8eafd-c2f5-4c74-a525-bb107fababf6 | 1 | 2012-07-24 |
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 |
|---|---|---|---|---|---|---|
| ENBREL | ETANERCEPT | Immunex Corporation | a002b40c-097d-47a5-957f-7a7b1807af7f | 2026-05-11 | Boxed warning, Warnings, Adverse reactions | BLA103795 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.