# HYDROXYCHLOROQUINE SULFATE

NDC: 50268-412
Generic name: HYDROXYCHLOROQUINE SULFATE
Labeler / Manufacturer: AvPAK
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200515

FDA application: ANDA210441

## 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:"50268-412"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50268-412
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a5b3455a-e842-7d4b-e053-2995a90adee3