Anticoagulant Citrate Dextrose A

ANHYDROUS CITRIC ACID, DEXTROSE MONOHYDRATE, AND TRISODIUM CITRATE DIHYDRATE EXTRACORPOREAL HUMAN PRESCRIPTION DRUG

Anticoagulant Citrate Dextrose A is an FDA drug label for the active ingredient ANHYDROUS CITRIC ACID, DEXTROSE MONOHYDRATE, AND TRISODIUM CITRATE DIHYDRATE manufactured by Citra Labs LLC administered by EXTRACORPOREAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20230214.

Generic name
ANHYDROUS CITRIC ACID, DEXTROSE MONOHYDRATE, AND TRISODIUM CITRATE DIHYDRATE
Manufacturer
Citra Labs LLC
Product type
HUMAN PRESCRIPTION DRUG
Route
EXTRACORPOREAL
Dosage form
N/A
NDC
23731-6051
Application
BN020037
Label effective
20230214

About this product

Anticoagulant Citrate Dextrose A is an FDA-registered drug product whose active ingredient is ANHYDROUS CITRIC ACID, DEXTROSE MONOHYDRATE, AND TRISODIUM CITRATE DIHYDRATE. It is labelled by Citra Labs LLC taken by extracorporeal and marketed as a human prescription drug product. Identifiers on file: NDC 23731-6051, application BN020037, label effective 20230214. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

What it is used for

Across FDA labelling, products containing ANHYDROUS CITRIC ACID, DEXTROSE MONOHYDRATE, AND TRISODIUM CITRATE DIHYDRATE are most often described in connection with: autologous prp, usage anticoagulant, citrate dextrose, solution solution, acd-a intended, extracorporeal blood, systems production, platelet rich. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Indications & Usage

Indications and Usage Anticoagulant Citrate Dextrose Solution, Solution A, U.S.P. (ACD-A), is intended for use as an anticoagulant in the extracorporeal blood processing with Autologous PRP Systems in production of platelet rich plasma (PRP). Refer to the manufacturer's Operator's Manual of the Autologous PRP System for the Directions for Use.

Dosage & Administration

Dosage and Administration Refer to the manufacturer's Operator's Manual of the Autologous PRP System for the Directions for Use.

Contraindications

Contraindications NOT FOR DIRECT INTRAVENOUS INFUSION

Warnings

Warnings NOT FOR DIRECT INTRAVENOUS INFUSION

Adverse Reactions

Adverse Reactions Not applicable. This product is used as an anticoagulant in the extracorporeal blood processing with Autologous PRP Systems in production of platelet rich plasma (PRP).

Frequently asked questions

What is Anticoagulant Citrate Dextrose A used for?
Indications and Usage Anticoagulant Citrate Dextrose Solution, Solution A, U.S.P. (ACD-A), is intended for use as an anticoagulant in the extracorporeal blood processing with Autologous PRP Systems in production of platelet rich plasma (PRP). Refer to the manufacturer's Operator's Manual of the Autologous PRP System for the Directions for Use.

Who makes Anticoagulant Citrate Dextrose A?
Citra Labs LLC is the labeler of record for Anticoagulant Citrate Dextrose A.

What form does Anticoagulant Citrate Dextrose A come in?
administered by extracorporeal. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Anticoagulant Citrate Dextrose A prescription or over-the-counter?
The FDA label for this product is recorded as human prescription drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Has Anticoagulant Citrate Dextrose A been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.