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Brand-name prescription medicine

Thiola EC

Generic name: Tiopronin

FDA application holder: Mission Pharmacal

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 Thiola EC?
Thiola EC is a brand name of Tiopronin, a prescription medicine. The FDA NDC Directory lists 2 Thiola EC products in 2 strengths and forms.
Who makes Thiola EC?
Mission Pharmacal holds the FDA application for Thiola EC (NDA211843, approved June 28, 2019).
Is there a generic or store brand of Thiola EC?
Yes. The FDA NDC Directory lists 11 other products with the same active ingredients, strength and form as a Thiola EC product, 11 of them generic. Ask your pharmacist whether one is right for you.
Has Thiola EC been recalled?
No recall linked to Thiola EC products (by their NDC code or label) appears in the FDA enforcement reports we use.

What Thiola EC is

Each Thiola EC 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.

Tiopronin · prescription medicine

Strength and formProduct namesSame medicine, other namesLabel
tiopronin 100 mg
tablet, delayed release (oral)
Thiola EC 5 products, 5 companies DailyMed
tiopronin 300 mg
tablet, delayed release (oral)
Thiola EC 6 products, 6 companies DailyMed

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

FDA approval

  • NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
FDA applications of Thiola EC products (Drugs@FDA)
ApplicationHolderFirst approvedProducts
NDA211843Mission PharmacalJune 28, 20192

Companies that list Thiola EC

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

Recalls

No recall linked to Thiola EC 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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