Leukotrap WB System
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- Leukotrap WB System
- Generic name
- CPDA-1 BLOOD BAG COLLECTION SYSTEM
- Manufacturer
- GVS TM INC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 54fdf83e-f641-1f69-e063-6394a90ab750
- SPL ID
- 54fdf83e-f642-1f69-e063-6394a90ab750
- Version
- 1
- Effective date
- 2026-06-24
- Source export date
- 2026-10-12
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
- Import run
- 20261013T011858Z
- Imported at
- 2026-10-13 02:56:37
| Harmonized routes |
|---|
| INTRAVENOUS |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application number | BN800077 | openfda.application_number | |
| brand name | Leukotrap WB System | openfda.brand_name | |
| generic name | CPDA-1 BLOOD BAG COLLECTION SYSTEM | openfda.generic_name | |
| manufacturer name | GVS TM INC | openfda.manufacturer_name | |
| ndc | package | 87069-736-62 | openfda.package_ndc |
| ndc | product | 87069-736 | openfda.product_ndc |
| ndc11 | package | 87069073662 | derived:openfda.package_ndc |
| spl id | 54fdf83e-f642-1f69-e063-6394a90ab750 | id | |
| spl set id | 54fdf83e-f641-1f69-e063-6394a90ab750 | set_id | |
| unii | JAC85A2161 | openfda.unii | |
| unii | 2968PHW8QP | openfda.unii | |
| unii | 1Q73Q2JULR | openfda.unii | |
| unii | LX22YL083G | openfda.unii | |
| unii | 593YOG76RN | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.