Quick answers
- What is Venxxiva?
- Venxxiva is a brand name of Tiopronin, a prescription medicine. The FDA NDC Directory lists 2 Venxxiva products in 2 strengths and forms.
- Who makes Venxxiva?
- Torrent holds the FDA application for Venxxiva (ANDA216990, approved January 30, 2024).
- Is there a generic or store brand of Venxxiva?
- Yes. The FDA NDC Directory lists 11 other products with the same active ingredients, strength and form as a Venxxiva product, 9 of them generic. Ask your pharmacist whether one is right for you.
- Has Venxxiva been recalled?
- No recall linked to Venxxiva products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Venxxiva is
Each Venxxiva 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 form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| tiopronin 100 mg tablet, delayed release (oral) | Venxxiva | 5 products, 5 companies | DailyMed |
| tiopronin 300 mg tablet, delayed release (oral) | Venxxiva | 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
- ANDA: Abbreviated New Drug Application: how a generic version is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| ANDA216990 | Torrent | January 30, 2024 | 2 |
Companies that list Venxxiva
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Venxxiva products.
- Cycle Pharmaceuticals Ltd.2 products
Recalls
No recall linked to Venxxiva products (by their NDC code or label) appears in the FDA enforcement reports.
Sources
- NDC Directory (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drugs@FDA (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug labeling (SPL, openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 30, 2026, retrieved October 31, 2026
- Drug recall enforcement reports (openFDA) — U.S. Food and Drug Administration (FDA), FDA data exported October 27, 2026, retrieved October 31, 2026
- 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.