SOVUNA 300 mg/1

Hydroxychloroquine Sulfate · TABLET, FILM COATED · ANI Pharmaceuticals, Inc.

No Recall HistoryCurrently in Shortage

Plain English

Sovuna is a prescription tablet containing hydroxychloroquine sulfate, which is used to treat conditions such as malaria, lupus, and rheumatoid arthritis. It works by reducing inflammation and modulating the immune system's response in the body.

Key Facts

Brand Name: SOVUNA
Generic Name: Hydroxychloroquine Sulfate
NDC Code (Product): 70954-805
Manufacturer: ANI Pharmaceuticals, Inc.
Strength: 300 mg/1
Dosage Form: TABLET, FILM COATED
Route: ORAL
Marketing Status
Application #: NDA214581
Marketing Start: 09/15/2023

Recall History

No Recall History

Side Effects Reported to FDA

FDA FAERS database · These are reported events, not confirmed side effects

drug ineffective18,095 reports

rheumatoid arthritis13,674 reports

pain10,809 reports

fatigue9,379 reports

drug intolerance9,240 reports

off label use8,457 reports

joint swelling8,397 reports

arthralgia8,376 reports

contraindicated product administered8,075 reports

alopecia7,711 reports

Frequently Asked Questions

What is SOVUNA used for?

Is SOVUNA a controlled substance?

SOVUNA is not classified as a controlled substance by the DEA.

What is the generic name for SOVUNA?

The generic name for SOVUNA is Hydroxychloroquine Sulfate. There are 11 other brand versions of Hydroxychloroquine Sulfate.

What is the NDC code for SOVUNA 300 mg/1?

The NDC (National Drug Code) for SOVUNA 300 mg/1 is 70954-805, listed by ANI Pharmaceuticals, Inc..

Product NDC

70954-805

Package NDC

70954-805-10

Other SOVUNA Dosages

SOVUNA200 mg/1
70954-804

Other Hydroxychloroquine Brands

See all →

Not medical advice. Always consult your doctor or pharmacist before making any medication decisions.

Data from openFDA · Public domain (CC0 1.0)