Anticoagulant Citrate Dextrose A ACD-A
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
- Anticoagulant Citrate Dextrose A ACD-A
- Generic name
- ANTICOAGULANT CITRATE DEXTROSE A ACD-A
- Manufacturer
- Arteriocyte Medical Systems, Inc.
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- b850deac-161f-4bb0-ac7f-bceac2a230c0
- SPL ID
- 49c60185-a86d-44a7-a10e-d0ec57df1fbe
- Version
- 4
- Effective date
- 2025-01-23
- Source export date
- 2026-11-06
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/9d5577a314a25811fefbde4767c9b37f3913d9a65fdc458c6336b5aed532339e/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- 8dff71fbef1291eb7711013e9a3a06194930757924a8946ae3034107a98d9463
- Import run
- 20261106T075659Z
- Imported at
- 2026-11-06 08:51:24
| Harmonized routes |
|---|
| EXTRACORPOREAL |
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 | BA110057 | openfda.application_number | |
| brand name | Anticoagulant Citrate Dextrose A ACD-A | openfda.brand_name | |
| generic name | ANTICOAGULANT CITRATE DEXTROSE A ACD-A | openfda.generic_name | |
| manufacturer name | Arteriocyte Medical Systems, Inc. | openfda.manufacturer_name | |
| ndc | package | 43203-852-47 | openfda.package_ndc |
| ndc | product | 43203-852 | openfda.product_ndc |
| ndc11 | package | 43203085247 | derived:openfda.package_ndc |
| spl id | 49c60185-a86d-44a7-a10e-d0ec57df1fbe | id | |
| spl set id | b850deac-161f-4bb0-ac7f-bceac2a230c0 | set_id | |
| unii | 2968PHW8QP | openfda.unii | |
| unii | 1Q73Q2JULR | openfda.unii | |
| unii | LX22YL083G | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.