# SOVUNA

NDC: 70954-804
Generic name: Hydroxychloroquine Sulfate
Labeler / Manufacturer: ANI Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20230915

FDA application: NDA214581

## Active ingredients

- HYDROXYCHLOROQUINE SULFATE: 200 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70954-804"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70954-804
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dd441154-b196-4d4c-bc56-2e37f345ef8d