# HYDROXYCHLOROQUINE SULFATE

NDC: 59651-889
Generic name: HYDROXYCHLOROQUINE SULFATE
Labeler / Manufacturer: Aurobindo Pharma Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20250307

FDA application: ANDA040274

## 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:"59651-889"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=59651-889
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e6f889ff-c5ba-4324-b87c-ec3ac942be2f