# CHLORTHALIDONE CHLORTHALIDONE

NDC: 46708-676
Generic name: CHLORTHALIDONE
Labeler / Manufacturer: Alembic Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20220829

FDA application: ANDA216262

## Active ingredients

- CHLORTHALIDONE: 25 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"46708-676"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=46708-676
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1b98d1a1-9d3d-41d2-a5e9-744b851d30d4