NDC 82009-159 - Adalimumab-ryvk
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
- 82009-159
- Package NDCs from labels
- 82009-159-11
- Manufacturer
- Quallent Pharmaceuticals Health LLC | Alvotech HF
- Effective date
- 2026-01-19
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Adalimumab-ryvk - Quallent Pharmaceuticals Health LLC | Alvotech HF | Quallent Pharmaceuticals Health LLC | Alvotech HF | 2026-01-19 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 82009-159-11 | Adalimumab-ryvk | 0.4 mL in 1 SYRINGE | INJECTION, SOLUTION | 0.4 mL | 40 mg in 0.4mL | 12 |
| 82009-159-11 | Adalimumab-ryvk | 1 in 1 TRAY | INJECTION, SOLUTION | 40 mg in 0.4mL | 12 |
DailyMed Dashboard NDC Coverage#
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.
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| Sterile Water | WATER INJECTION | Henry Schein, Inc. | 3501952b-b556-4d5e-b81b-5c35ff87b475 | 2025-08-28 | Warnings, Adverse reactions | 059QF0KO0R |
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Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.