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Brand-name prescription medicine

LMD in Dextrose

Generic name: Dextran 40

Company: Hospira, 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 LMD in Dextrose?
LMD in Dextrose is a brand name of Dextran 40, a prescription medicine. The FDA NDC Directory lists 1 LMD in Dextrose product in 1 strength and form.
Who makes LMD in Dextrose?
Hospira, Inc. lists 1 of the 1 LMD in Dextrose products in the FDA NDC Directory.
Is there a generic or store brand of LMD in Dextrose?
Yes. The FDA NDC Directory lists 1 other product with the same active ingredients, strength and form as a LMD in Dextrose product, 1 of them generic. Ask your pharmacist whether one is right for you.
Has LMD in Dextrose been recalled?
FDA enforcement reports list 1 recall of LMD in Dextrose products; the newest started October 2, 2019. A recall usually concerns specific lots, not every product.

What LMD in Dextrose is

Each LMD in Dextrose 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.

Dextran 40 · prescription medicine

Strength and formProduct namesSame medicine, other namesLabel
dextran 40 10%
injection, solution (intravenous)
LMD in Dextrose 1 product, 1 company DailyMed

Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Dextran 40 →

FDA approval

No Drugs@FDA application is linked to these products.

Companies that list LMD in Dextrose

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

Recalls

From FDA enforcement reports, matched by the product’s NDC code or label. A recall usually covers specific lots: check the lot number on your package and ask your pharmacist. Do not stop a medicine on your own.

  1. October 2, 2019 · Class II · Terminated · D-0136-2020

    Lack of Assurance of Sterility: Bag has the potential to leak.

    10% LMD in 5% Dextrose Injection Dextran 40 in Dextrose Injection, USP, 500 mL bags, Rx only, Hospira, Inc., Lake Forest, IL 60045, NDC 0409-7418-13 — Pfizer Inc.

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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