# Hydroxychloroquine Sulfate

NDC: 60219-1544
Generic name: Hydroxychloroquine Sulfate
Labeler / Manufacturer: Amneal Pharmaceuticals NY LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20180517

FDA application: ANDA210577

## 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:"60219-1544"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60219-1544
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6a9e2fc8-bedf-46d4-9973-328dbcb18061