acd-a

Generic: anticoagulant citrate dextrose solution formula a

Labeler: fenwal, inc.
NDC Directory HUMAN PRESCRIPTION DRUG NDA Inactive Finished

Drug Facts

Product Profile

Brand Name acd-a
Generic Name anticoagulant citrate dextrose solution formula a
Labeler fenwal, inc.
Dosage Form SOLUTION
Routes
INTRAVENOUS
Active Ingredients

anhydrous citric acid 3.65 g/500mL, dextrose monohydrate 12.25 g/500mL, sodium citrate, unspecified form 11 g/500mL

Manufacturer
Fenwal, Inc.

Identifiers & Regulatory

Product NDC 0942-0641
Product ID 0942-0641_fc8f1ca0-251a-493a-ad8e-defe2a5c7141
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category NDA
Application Number BN160918
Listing Expiration 2026-12-31
Marketing Start 2007-03-01

Pharmacologic Class

Established (EPC)
calculi dissolution agent [epc] anti-coagulant [epc]
Mechanism of Action
acidifying activity [moa] calcium chelating activity [moa]
Physiologic Effect
decreased coagulation factor activity [pe]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 09420641
Hyphenated Format 0942-0641

Supplemental Identifiers

UNII
XF417D3PSL LX22YL083G 1Q73Q2JULR
NUI
N0000175833 N0000175835 N0000175980 N0000008556 N0000175089

Packaging Origin

Original Packager
true

Resolved Product View

Precedence rule: structured NDC data is preferred, falling back to linked label metadata when unavailable. Source tags show the origin of each value.

Resolved Identity

Brand Name acd-a (source: ndc)
Generic Name anticoagulant citrate dextrose solution formula a (source: ndc)
Application Number BN160918 (source: ndc)
Routes
INTRAVENOUS
source: ndc

Resolved Composition

Strengths
  • 3.65 g/500mL
  • 12.25 g/500mL
  • 11 g/500mL
source: ndc
Packaging
  • 500 mL in 1 BAG (0942-0641-03)
source: ndc

Packages (1)

0942-0641-03 500 mL in 1 BAG (0942-0641-03)

Ingredients (3)

anhydrous citric acid (3.65 g/500mL) dextrose monohydrate (12.25 g/500mL) sodium citrate, unspecified form (11 g/500mL)

Linked Drug Pages (2)

ACD-A ndc-match (0.9) ACD-A ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["INTRAVENOUS"], "spl_id": "fc8f1ca0-251a-493a-ad8e-defe2a5c7141", "openfda": {"nui": ["N0000175833", "N0000175835", "N0000175980", "N0000008556", "N0000175089"], "unii": ["XF417D3PSL", "LX22YL083G", "1Q73Q2JULR"], "spl_set_id": ["22805f0d-ba58-41ea-b245-19980abcda22"], "pharm_class_pe": ["Decreased Coagulation Factor Activity [PE]"], "pharm_class_epc": ["Calculi Dissolution Agent [EPC]", "Anti-coagulant [EPC]"], "pharm_class_moa": ["Acidifying Activity [MoA]", "Calcium Chelating Activity [MoA]"], "manufacturer_name": ["Fenwal, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "500 mL in 1 BAG (0942-0641-03)", "package_ndc": "0942-0641-03", "marketing_start_date": "20070301"}], "brand_name": "ACD-A", "product_id": "0942-0641_fc8f1ca0-251a-493a-ad8e-defe2a5c7141", "dosage_form": "SOLUTION", "pharm_class": ["Acidifying Activity [MoA]", "Acidifying Activity [MoA]", "Anti-coagulant [EPC]", "Anti-coagulant [EPC]", "Calcium Chelating Activity [MoA]", "Calcium Chelating Activity [MoA]", "Calculi Dissolution Agent [EPC]", "Calculi Dissolution Agent [EPC]", "Decreased Coagulation Factor Activity [PE]", "Decreased Coagulation Factor Activity [PE]"], "product_ndc": "0942-0641", "generic_name": "Anticoagulant Citrate Dextrose Solution Formula A", "labeler_name": "Fenwal, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "ACD-A", "active_ingredients": [{"name": "ANHYDROUS CITRIC ACID", "strength": "3.65 g/500mL"}, {"name": "DEXTROSE MONOHYDRATE", "strength": "12.25 g/500mL"}, {"name": "SODIUM CITRATE, UNSPECIFIED FORM", "strength": "11 g/500mL"}], "application_number": "BN160918", "marketing_category": "NDA", "marketing_start_date": "20070301", "listing_expiration_date": "20261231"}