Quick answers
- What is InterSol?
- 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) and Platelet additive 3 (sodium acetate / sodium chloride / sodium phosphate, dibasic / sodium phosphate, monobasic, monohydrate / trisodium citrate dihydrate), a prescription medicine. The FDA NDC Directory lists 3 InterSol products in 2 strengths and forms.
- Who makes InterSol?
- Fenwal, Inc. lists 3 of the 3 InterSol products in the FDA NDC Directory.
- Is there a generic or store brand of InterSol?
- Yes. The FDA NDC Directory lists 1 other product with the same active ingredients, strength and form as a InterSol product. Ask your pharmacist whether one is right for you.
- Has InterSol been recalled?
- No recall linked to InterSol products (by their NDC code or label) appears in the FDA enforcement reports we use.
What InterSol is
Each 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 form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| 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) | InterSol | 1 product, 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) →
Platelet additive 3 (sodium acetate / sodium chloride / sodium phosphate, dibasic / sodium phosphate, monobasic, monohydrate / trisodium citrate dihydrate) · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| sodium acetate 442 mg/100 mL · sodium chloride 452 mg/100 mL · sodium phosphate, dibasic 305 mg/100 mL · sodium phosphate, monobasic, monohydrate 93 mg/100 mL · trisodium citrate dihydrate 318 mg/100 mL solution (intravenous) | InterSol | None listed | 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 / sodium phosphate, monobasic, monohydrate / trisodium citrate dihydrate) →
FDA approval
No Drugs@FDA application is linked to these products.
Companies that list InterSol
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of InterSol products.
- Fenwal, Inc.3 products
Recalls
No recall linked to InterSol products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- 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.