NDC 68982-350-81 - Fibryga
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
- 68982-350
- Requested NDC
- 68982-350-81
- Package NDCs from labels
- 68982-350-81, 68982-350-01
- Manufacturer
- Octapharma USA Inc
- Effective date
- 2025-08-05
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Fibryga - Octapharma USA Inc | Octapharma USA Inc | 2025-08-05 | PLASMA DERIVATIVE |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 68982-350-01 | Fibryga | 1 in 1 CARTON | POWDER, FOR SOLUTION | 1 | 4 | |
| 68982-350-81 | Fibryga | 100 mL in 1 BOTTLE, GLASS | POWDER, FOR SOLUTION | 100 | 4 |
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 68982-350-01 | EA - Each | 68982-350 | 972a65f6-4874-4a36-867a-4397aa853ae2 | 1 | 2025-10-14 |
| 68982-350-81 | EA - Each | 68982-350 | 6a0aef4f-77ff-4e85-a08a-617d61a341f5 | 1 | 2025-10-14 |
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 |
|---|---|---|---|---|---|---|
| TachoSil | THROMBIN HUMAN AND FIBRINOGEN | Corza Medical GmbH | 0c324332-290f-413f-820c-8c9a971a2766 | 2025-10-08 | Warnings, Adverse reactions | N94833051K |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.