NDC 86184-318-01 - PROTIRELIN
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
- 86184-318
- Requested NDC
- 86184-318-01
- Package NDCs from labels
- 86184-318-01
- Manufacturer
- MAEDA INC
- Effective date
- 2026-03-23
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| PROTIRELIN - MAEDA INC | MAEDA INC | 2026-03-23 | BULK INGREDIENT - ANIMAL DRUG |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 86184-318-01 | PROTIRELIN | 1 g in 1 PACKAGE | POWDER | 1 | 1 |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.