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Brand-name prescription medicine

Solucion InterSol

Generic name: Platelet additive 3 (sodium acetate / sodium chloride / sodium phosphate, dibasic, unspecified form / sodium phosphate, monobasic, monohydrate / trisodium citrate dihydrate)

Company: Fenwal, Inc.

Official data, not advice

Everything here comes from the U.S. Food and Drug Administration (FDA): the NDC Directory, Drugs@FDA, the official labels and recall reports; pharmacy costs come from the Centers for Medicare & Medicaid Services (CMS). Each fact shows its source and date.

This page is not medical advice. Talk to your doctor or pharmacist before you start, stop or switch any medicine, including a switch between a brand and a generic.

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

Quick answers

What is Solucion InterSol?
Solucion InterSol is a brand name of Platelet additive 3 (sodium acetate / sodium chloride / sodium phosphate, dibasic, unspecified form / sodium phosphate, monobasic, monohydrate / trisodium citrate dihydrate), a prescription medicine. The FDA NDC Directory lists 1 Solucion InterSol product in 1 strength and form.
Who makes Solucion InterSol?
Fenwal, Inc. lists 1 of the 1 Solucion InterSol products in the FDA NDC Directory.
Is there a generic or store brand of Solucion InterSol?
Yes. The FDA NDC Directory lists 2 other products with the same active ingredients, strength and form as a Solucion InterSol product. Ask your pharmacist whether one is right for you.
Has Solucion InterSol been recalled?
No recall linked to Solucion InterSol products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Solucion InterSol is

Each Solucion InterSol product as listed in the FDA NDC Directory, by active ingredient, strength and form, with its official label. “Same medicine, other names” counts the other products with exactly the same active ingredients, strength and form (generic versions, store brands and other brands); inactive ingredients can differ.

Platelet additive 3 (sodium acetate / sodium chloride / sodium phosphate, dibasic, unspecified form / sodium phosphate, monobasic, monohydrate / trisodium citrate dihydrate) · prescription medicine

Strength and formProduct namesSame medicine, other namesLabel
sodium acetate 442 mg/100 mL · sodium chloride 452 mg/100 mL · sodium phosphate, dibasic, unspecified form 305 mg/100 mL · sodium phosphate, monobasic, monohydrate 93 mg/100 mL · trisodium citrate dihydrate 318 mg/100 mL
solution (intravenous)
Solucion InterSol 2 products, 1 company DailyMed

Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Platelet additive 3 (sodium acetate / sodium chloride / sodium phosphate, dibasic, unspecified form / sodium phosphate, monobasic, monohydrate / trisodium citrate dihydrate) →

FDA approval

No Drugs@FDA application is linked to these products.

Companies that list Solucion InterSol

The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Solucion InterSol products.

Recalls

No recall linked to Solucion InterSol products (by their NDC code or label) appears in the FDA enforcement reports.

Sources

  1. NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  2. Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
  3. Drug labeling (SPL, 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. NADAC (National Average Drug Acquisition Cost) 2026 — Centers for Medicare & Medicaid Services (CMS), data.medicaid.gov, list of November 4, 2026, retrieved November 7, 2026

Which names get a brand page: a name the NDC Directory lists for a medicine, held by one company (the FDA application holder, or the company named on most of its products), that is not just a description, and that is not the only product of its medicine.

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