Leukotrap RC System

Leukotrap RC System is an FDA-registered drug product whose active ingredient is CP2D/AS-3 ANTICOAGULANT AND ADDITIVE SYSTEM. It is labelled by GVS TM INC taken by intravenous and marketed as a human prescription drug product. Identifiers on file: NDC 87069-129, application BN820915, label effective 20260703. It is one of 8 FDA drug label records sharing the active ingredient CP2D/AS-3 ANTICOAGULANT AND ADDITIVE SYSTEM. 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.

FDA lists 8 drug label records with CP2D/AS-3 ANTICOAGULANT AND ADDITIVE SYSTEM as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

What is Leukotrap RC System used for?
No indications section is present in the FDA label on file for this product. Consult the prescribing information supplied with the medicine or ask a pharmacist.

Who makes Leukotrap RC System?
GVS TM INC is the labeler of record for Leukotrap RC System. 8 FDA label records share the active ingredient CP2D/AS-3 ANTICOAGULANT AND ADDITIVE SYSTEM, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does Leukotrap RC System come in?
administered by intravenous. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is Leukotrap RC System 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.

Are there other products containing CP2D/AS-3 ANTICOAGULANT AND ADDITIVE SYSTEM?
Yes. 8 FDA drug label records list CP2D/AS-3 ANTICOAGULANT AND ADDITIVE SYSTEM as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has Leukotrap RC System 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.