# Hydroxychloroquine sulfate

NDC: 65841-633
Generic name: Hydroxychloroquine sulfate
Labeler / Manufacturer: Zydus Lifesciences Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20080103

FDA application: ANDA040657

## 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:"65841-633"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=65841-633
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1aa44bff-9a62-48b4-a520-98d7d524e3a9