# Chlorthalidone

NDC: 57664-649
Generic name: Chlorthalidone
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20160212

FDA application: ANDA089286

## Active ingredients

- CHLORTHALIDONE: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"57664-649"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=57664-649
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a304de67-cd2b-4933-937e-4eeecf6cda40