# HYDROXYCHLOROQUINE SULFATE

NDC: 82619-131
Generic name: hydroxychloroquine sulfate
Labeler / Manufacturer: Creekwood Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250508

FDA application: ANDA040150

## 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:"82619-131"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=82619-131
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=04139607-f7c0-4fe1-a210-ffa5af347d56