NDC 53877-110-01 - teruflex blood bag system with diversion blood sampling arm 70 ml cpda-1
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
- 53877-110
- Requested NDC
- 53877-110-01
- Package NDCs from labels
- 53877-110-02, 53877-110-01, 53877-110-06
- Manufacturer
- Terumo Corporation | Terumo Corp. - Fujinomiya Factory
- Effective date
- 2024-10-10
- Current FDA listing
- Not matched in FDA.report NDC product tables
DailyMed Labels#
| Label | Manufacturer | Effective date | Type |
|---|---|---|---|
| Anhydrous Citric Acid - Terumo Corporation | Terumo Corp. - Fujinomiya Factory | Terumo Corporation | Terumo Corp. - Fujinomiya Factory | 2024-10-10 | HUMAN PRESCRIPTION DRUG LABEL |
DailyMed Package Descriptions#
| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|---|---|---|---|---|---|
| 53877-110-01 | teruflex blood bag system with diversion blood sampling arm 70 ml cpda-1 | 5 in 1 BLISTER PACK | SOLUTION | 5 | 1 | |
| 53877-110-02 | teruflex blood bag system with diversion blood sampling arm 70 ml cpda-1 | 70 mL in 1 BAG | SOLUTION | 70 | 1 | |
| 53877-110-06 | teruflex blood bag system with diversion blood sampling arm 70 ml cpda-1 | 6 in 1 CASE | SOLUTION | 6 | 1 |
DailyMed Dashboard NDC Coverage#
| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|---|---|---|---|
| 53877-110 | TERUFLEX BLOOD BAG SYSTEM WITH DIVERSION BLOOD SAMPLING ARM 70 ML CPDA-1 (ANHYDROUS CITRIC ACID, TRISODIUM CITRATE DIHYDRATE, SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE, DEXTROSE MONOHYDRATE, AND ADENINE) SOLUTION [TERUMO CORPORATION] | 1 | Current NDC, 3 package rows | 20241012_86b3a329-c83f-4977-92f5-0e9dfe1872d7.zip |
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.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.