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Brand-name prescription medicine

Wezlana

Generic name: Ustekinumab

FDA application holder: Amgen Inc

Strengths and generic versions Official label

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.

At a glance

3Strengths and forms
26Same medicine, other names
2023FDA approval
0Recalls (FDA reports)

Quick answers

What is Wezlana?
Wezlana is a brand name of Ustekinumab, a prescription medicine. The FDA NDC Directory lists 7 Wezlana products in 3 strengths and forms.
Who makes Wezlana?
Amgen Inc holds the FDA application for Wezlana (BLA761285, approved October 31, 2023).
Is there a generic or store brand of Wezlana?
Yes. The FDA NDC Directory lists 26 other products with the same active ingredients, strength and form as a Wezlana product. Ask your pharmacist whether one is right for you.
Has Wezlana been recalled?
No recall linked to Wezlana products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Wezlana is

Each Wezlana 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.

Ustekinumab · prescription medicine

Strength and formProduct namesSame medicine, other namesLabel
ustekinumab 130 mg/26 mL
injection, solution (intravenous)		 Wezlana 3 products, 3 companies DailyMed
ustekinumab 45 mg/0.5 mL
injection, solution (subcutaneous)		 Wezlana 13 products, 7 companies DailyMed
ustekinumab 90 mg/mL
injection, solution (subcutaneous)		 Wezlana 10 products, 8 companies DailyMed

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

FDA approval

  • BLA: Biologics License Application: how a biologic medicine (made from living cells) is approved.
FDA applications of Wezlana products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
BLA761285Amgen IncOctober 31, 20236
BLA761331Amgen IncOctober 31, 20231

Companies that list Wezlana

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

Recalls

No recall linked to Wezlana 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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