# HYDROXYCHLOROQUINE SULFATE

NDC: 43598-133
Generic name: HYDROXYCHLOROQUINE SULFATE
Labeler / Manufacturer: Dr. Reddy's Laboratories Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20221024

FDA application: ANDA210441

## Active ingredients

- HYDROXYCHLOROQUINE SULFATE: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43598-133"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43598-133
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=452092b4-7a8f-4d19-8113-f1c2a948d3d8