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Prescription medicine

Anticoagulant citrate dextrose solution formula a

Brand names: Acd-A

Active ingredients: anhydrous citric acid · dextrose monohydrate · sodium citrate, unspecified form

Drug class: Calculi Dissolution Agent, Anti-coagulant

The FDA’s “Established Pharmacologic Class”: the group of medicines that work in a similar way.

Full FDA label All drugs

Official FDA data, not advice

Everything here comes from the U.S. Food and Drug Administration (FDA): the drug label, the NDC Directory, Drugs@FDA, recall reports and the drug shortage list. Each fact shows its source and date.

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.

In an emergency, call 911. If someone may have taken too much of a medicine, call Poison Help: 1‑800‑222‑1222.

At a glance

NoBoxed warning
None listedFDA shortage list
0Recalls (FDA reports)
1Companies

Quick answers

Does Anticoagulant citrate dextrose solution formula a have a boxed warning?
No. None of the 2 FDA labels we found for this medicine has a boxed warning.
Is there a shortage of Anticoagulant citrate dextrose solution formula a?
No current shortage is listed by the FDA for the products of this medicine (FDA data from October 30, 2026).
Has Anticoagulant citrate dextrose solution formula a been recalled?
No recall linked to the products of this medicine appears in the FDA enforcement reports we use.
Who makes Anticoagulant citrate dextrose solution formula a?
1 company lists prescription products of Anticoagulant citrate dextrose solution formula a in the FDA NDC Directory, including Fenwal, Inc..

What Anticoagulant citrate dextrose solution formula a is used for

We did not find an “Indications and Usage” section in the FDA labels for this medicine. See the label on DailyMed →

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or change any medicine.

Boxed warning

A boxed warning (“black box”) is the FDA’s strongest warning on a drug label, for serious or life-threatening risks.

The label quoted above has no boxed warning.

0 of 2 FDA labels for this medicine have a boxed warning.

Forms and how it is given

Dosage formsSolution
RouteIntravenous
Prescription products1 in the FDA NDC Directory
Brand namesAcd-A

Companies that list this medicine

Labelers in the FDA NDC Directory: the company named on the package (maker or distributor), with the number of prescription products.

FDA approval history

No Drugs@FDA application is linked to these products.

Shortage status

The FDA drug shortage list does not show these products.

FDA Drug Shortages database →

Recalls

No recall linked to these products (by their NDC code) appears in the FDA enforcement reports.

Official identifiers

SPL set ID of the quoted labelab19b011-0a51-4f04-9881-d9fc7cae95ae
FDA labels (SPL)2
Active ingredients (FDA)ANHYDROUS CITRIC ACID / DEXTROSE MONOHYDRATE / SODIUM CITRATE, UNSPECIFIED FORM

Sources

  1. FDA-approved label on DailyMed (National Library of Medicine) — Acd-A, Fenwal, Inc., effective November 25, 2025; via openFDA, FDA data exported October 30, 2026, retrieved October 31, 2026
  2. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  4. Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
  5. Drug shortages (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026

openFDA data is provided by the FDA as is; it may be incomplete. Always rely on the label that comes with your medicine. FDA Enforcement Report search →

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