Quick answers
- What is Sovuna?
- Sovuna is a brand name of Hydroxychloroquine sulfate, a prescription medicine. The FDA NDC Directory lists 2 Sovuna products in 2 strengths and forms.
- Who makes Sovuna?
- Novitium Pharma holds the FDA application for Sovuna (NDA214581, approved January 14, 2022).
- Is there a generic or store brand of Sovuna?
- Yes. The FDA NDC Directory lists 35 other products with the same active ingredients, strength and form as a Sovuna product, 35 of them generic. Ask your pharmacist whether one is right for you.
- Has Sovuna been recalled?
- No recall linked to Sovuna products (by their NDC code or label) appears in the FDA enforcement reports we use.
What Sovuna is
Each Sovuna 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.
Hydroxychloroquine sulfate · prescription medicine
| Strength and form | Product names | Same medicine, other names | Label |
|---|---|---|---|
| hydroxychloroquine sulfate 200 mg tablet, film coated (oral) | Sovuna | 34 products, 23 companies | DailyMed |
| hydroxychloroquine sulfate 300 mg tablet, film coated (oral) | Sovuna | 1 product, 1 company | DailyMed |
Its page lists every product and company, the FDA label’s uses and boxed warning, approvals, shortages and recalls: Hydroxychloroquine sulfate →
FDA approval
- NDA: New Drug Application: how a new (usually brand-name) medicine is approved.
| Application | Holder | First approved | Products |
|---|---|---|---|
| NDA214581 | Novitium Pharma | January 14, 2022 | 2 |
Companies that list Sovuna
The company named on the package (holder, repackager or distributor), as listed in the FDA NDC Directory, with its number of Sovuna products.
- ANI Pharmaceuticals, Inc.2 products
Recalls
No recall linked to Sovuna 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.