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Brand-name prescription medicine

Zosyn in Galaxy Containers

Generic name: Piperacillin and tazobactam

FDA application holder: Baxter Hlthcare Corp

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 Zosyn in Galaxy Containers?
Zosyn in Galaxy Containers is a brand name of Piperacillin and tazobactam, a prescription medicine. The FDA NDC Directory lists 3 Zosyn in Galaxy Containers products in 3 strengths and forms.
Who makes Zosyn in Galaxy Containers?
Baxter Hlthcare Corp holds the FDA application for Zosyn in Galaxy Containers (NDA050750, approved February 24, 1998).
Is there a generic or store brand of Zosyn in Galaxy Containers?
Yes. The FDA NDC Directory lists 3 other products with the same active ingredients, strength and form as a Zosyn in Galaxy Containers product. Ask your pharmacist whether one is right for you.
Has Zosyn in Galaxy Containers been recalled?
No recall linked to Zosyn in Galaxy Containers products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Zosyn in Galaxy Containers is

Each Zosyn in Galaxy Containers 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.

Piperacillin and tazobactam · prescription medicine

Strength and formProduct namesSame medicine, other namesLabel
piperacillin sodium 2 g/50 mL · tazobactam sodium 250 mg/50 mL
injection, solution (intravenous)
Zosyn in Galaxy Containers 1 product, 1 company DailyMed
piperacillin sodium 3 g/50 mL · tazobactam sodium 375 mg/50 mL
injection, solution (intravenous)
Zosyn in Galaxy Containers 1 product, 1 company DailyMed
piperacillin sodium 4% · tazobactam sodium 500 mg/100 mL
injection, solution (intravenous)
Zosyn in Galaxy Containers 1 product, 1 company DailyMed

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

FDA approval

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
FDA applications of Zosyn in Galaxy Containers products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
NDA050750Baxter Hlthcare CorpFebruary 24, 19983

Companies that list Zosyn in Galaxy Containers

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

Recalls

No recall linked to Zosyn in Galaxy Containers 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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