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Brand-name prescription medicine

Wellbutrin XL

Generic name: Bupropion

FDA application holder: Bausch

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

2Strengths and forms
125Same medicine, other names
2003FDA approval
0Recalls (FDA reports)

Quick answers

What is Wellbutrin XL?
Wellbutrin XL is a brand name of Bupropion, a prescription medicine. The FDA NDC Directory lists 2 Wellbutrin XL products in 2 strengths and forms.
Who makes Wellbutrin XL?
Bausch holds the FDA application for Wellbutrin XL (NDA021515, approved August 28, 2003).
Is there a generic or store brand of Wellbutrin XL?
Yes. The FDA NDC Directory lists 125 other products with the same active ingredients, strength and form as a Wellbutrin XL product, 125 of them generic. Ask your pharmacist whether one is right for you.
Has Wellbutrin XL been recalled?
No recall linked to Wellbutrin XL products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Wellbutrin XL is

Each Wellbutrin XL 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.

Bupropion · prescription medicine

Strength and formProduct namesSame medicine, other namesLabel
bupropion hydrochloride 150 mg
tablet, extended release (oral)		 Wellbutrin XL 76 products, 38 companies DailyMed
bupropion hydrochloride 300 mg
tablet, extended release (oral)		 Wellbutrin XL 49 products, 34 companies DailyMed

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

FDA approval

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
FDA applications of Wellbutrin XL products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
NDA021515BauschAugust 28, 20032

Companies that list Wellbutrin XL

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

Recalls

No recall linked to Wellbutrin XL 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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