# Chlorthalidone

NDC: 33342-426
Generic name: Chlorthalidone
Labeler / Manufacturer: Macleods Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260701

FDA application: ANDA212229

## Active ingredients

- CHLORTHALIDONE: 50 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"33342-426"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=33342-426
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5de362df-8fb9-4421-864c-7ea06339d6e7