NDC 0069-1061-01 - Cutaquig
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
- 0069-1061
- Requested NDC
- 0069-1061-01
- Package NDCs from labels
- 0069-1061-01, 0069-1061-02
- Manufacturer
- Pfizer Laboratories Div Pfizer Inc
- Effective date
- 2025-03-24
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Cutaquig - Pfizer Laboratories Div Pfizer Inc | Pfizer Laboratories Div Pfizer Inc | 2025-03-24 | PLASMA DERIVATIVE |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 0069-1061-01 | Cutaquig | 6 mL in 1 VIAL, GLASS | SOLUTION | 6 | 15 | |
| 0069-1061-02 | Cutaquig | 1 in 1 CARTON | SOLUTION | 1 | 15 |
DailyMed Dashboard NDC Coverage#
DailyMed Billing Units#
| Package NDC | Billing unit | Product NDC | DailyMed indexing SPL | SPL version | Effective |
|---|---|---|---|---|---|
| 0069-1061-01 | ML - Milliliter | 0069-1061 | c616b486-adeb-4121-ab6b-735dff17c9b1 | 1 | 2019-10-07 |
| 0069-1061-02 | ML - Milliliter | 0069-1061 | 25cb5b8c-0ad0-4f25-b513-fa29e32aab46 | 1 | 2019-10-07 |
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 |
|---|---|---|---|---|---|---|
| QIVIGY kthm | HUMAN IMMUNOGLOBULIN G | Kedrion S.p.A. | 6f1933e0-240f-48f4-b246-8a30e63a4160 | 2026-02-02 | Boxed warning, Warnings, Adverse reactions | 66Y330CJHS |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.