CPDA-1
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
- CPDA-1
- Generic name
- ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINE
- Manufacturer
- Fenwal, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- d763511e-f1a7-4014-94b9-f7ad8f023ff4
- SPL ID
- e2fe6938-ea4c-490f-bee2-70a5d59a9c07
- Version
- 8
- Effective date
- 2021-12-02
- Source export date
- 2026-10-27
- Source partition
- 7
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/be847f9aea8d80a2cb7e9771acd1143be084664192ecf8f5be8ac1024116f4f0/drug-label-0007-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:15:30
| 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 | BN770420 | openfda.application_number | |
| brand name | CPDA-1 | openfda.brand_name | |
| generic name | ANTICOAGULANT CITRATE PHOSPHATE DEXTROSE ADENINE | openfda.generic_name | |
| manufacturer name | Fenwal, Inc. | openfda.manufacturer_name | |
| ndc | package | 0942-9393-02 | openfda.package_ndc |
| ndc | product | 0942-9393 | openfda.product_ndc |
| ndc11 | package | 00942939302 | derived:openfda.package_ndc |
| spl id | e2fe6938-ea4c-490f-bee2-70a5d59a9c07 | id | |
| spl set id | d763511e-f1a7-4014-94b9-f7ad8f023ff4 | set_id | |
| unii | JAC85A2161 | openfda.unii | |
| unii | XF417D3PSL | openfda.unii | |
| unii | B22547B95K | 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.