anticoagulant citrate dextrose a acd-a

Generic: anticoagulant citrate dextrose a acd-a

Labeler: arteriocyte medical systems, inc.
NDC Directory HUMAN PRESCRIPTION DRUG ANDA Inactive Finished

Drug Facts

Product Profile

Brand Name anticoagulant citrate dextrose a acd-a
Generic Name anticoagulant citrate dextrose a acd-a
Labeler arteriocyte medical systems, inc.
Dosage Form INJECTION, SOLUTION
Routes
EXTRACORPOREAL
Active Ingredients

citric acid monohydrate .08 g/10mL, dextrose monohydrate .245 g/10mL, sodium citrate, unspecified form .22 g/10mL

Manufacturer
Arteriocyte Medical Systems, Inc.

Identifiers & Regulatory

Product NDC 43203-852
Product ID 43203-852_49c60185-a86d-44a7-a10e-d0ec57df1fbe
Product Type HUMAN PRESCRIPTION DRUG
Marketing Category ANDA
Application Number BA110057
Listing Expiration 2026-12-31
Marketing Start 2011-05-11

Pharmacologic Class

Classes
acidifying activity [moa] anti-coagulant [epc] calcium chelating activity [moa] calculi dissolution agent [epc] decreased coagulation factor activity [pe] increased large intestinal motility [pe] inhibition large intestine fluid/electrolyte absorption [pe] osmotic activity [moa] osmotic laxative [epc]

Normalized Code Variants

Searchable formats for this product NDC code

Digits Only 43203852
Hyphenated Format 43203-852

Supplemental Identifiers

UNII
2968PHW8QP LX22YL083G 1Q73Q2JULR

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 anticoagulant citrate dextrose a acd-a (source: ndc)
Generic Name anticoagulant citrate dextrose a acd-a (source: ndc)
Application Number BA110057 (source: ndc)
Routes
EXTRACORPOREAL
source: ndc

Resolved Composition

Strengths
  • .08 g/10mL
  • .245 g/10mL
  • .22 g/10mL
source: ndc
Packaging
  • 50 POUCH in 1 CASE (43203-852-47) / 1 BAG in 1 POUCH / 50 mL in 1 BAG
source: ndc

Packages (1)

43203-852-47 50 POUCH in 1 CASE (43203-852-47) / 1 BAG in 1 POUCH / 50 mL in 1 BAG

Ingredients (3)

citric acid monohydrate (.08 g/10mL) dextrose monohydrate (.245 g/10mL) sodium citrate, unspecified form (.22 g/10mL)

Linked Drug Pages (1)

Anticoagulant Citrate Dextrose A ACD-A ndc-match (0.9)

Raw FDA Data

View complete raw FDA NDC JSON payload 
{"route": ["EXTRACORPOREAL"], "spl_id": "49c60185-a86d-44a7-a10e-d0ec57df1fbe", "openfda": {"unii": ["2968PHW8QP", "LX22YL083G", "1Q73Q2JULR"], "spl_set_id": ["b850deac-161f-4bb0-ac7f-bceac2a230c0"], "manufacturer_name": ["Arteriocyte Medical Systems, Inc."], "is_original_packager": [true]}, "finished": true, "packaging": [{"sample": false, "description": "50 POUCH in 1 CASE (43203-852-47)  / 1 BAG in 1 POUCH / 50 mL in 1 BAG", "package_ndc": "43203-852-47", "marketing_start_date": "20110511"}], "brand_name": "Anticoagulant Citrate Dextrose A ACD-A", "product_id": "43203-852_49c60185-a86d-44a7-a10e-d0ec57df1fbe", "dosage_form": "INJECTION, SOLUTION", "pharm_class": ["Acidifying Activity [MoA]", "Anti-coagulant [EPC]", "Calcium Chelating Activity [MoA]", "Calculi Dissolution Agent [EPC]", "Decreased Coagulation Factor Activity [PE]", "Increased Large Intestinal Motility [PE]", "Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]", "Osmotic Activity [MoA]", "Osmotic Laxative [EPC]"], "product_ndc": "43203-852", "generic_name": "Anticoagulant Citrate Dextrose A ACD-A", "labeler_name": "Arteriocyte Medical Systems, Inc.", "product_type": "HUMAN PRESCRIPTION DRUG", "brand_name_base": "Anticoagulant Citrate Dextrose A ACD-A", "active_ingredients": [{"name": "CITRIC ACID MONOHYDRATE", "strength": ".08 g/10mL"}, {"name": "DEXTROSE MONOHYDRATE", "strength": ".245 g/10mL"}, {"name": "SODIUM CITRATE, UNSPECIFIED FORM", "strength": ".22 g/10mL"}], "application_number": "BA110057", "marketing_category": "ANDA", "marketing_start_date": "20110511", "listing_expiration_date": "20261231"}