# HYDROXYCHLOROQUINE SULFATE

NDC: 42385-971
Generic name: HYDROXYCHLOROQUINE SULFATE
Labeler / Manufacturer: Laurus Labs Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20230306

FDA application: ANDA210959

## Active ingredients

- HYDROXYCHLOROQUINE SULFATE: 200 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42385-971"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42385-971
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=04d8fdbf-8829-4469-a341-8af2a2d91ccc