# IRBESARTAN AND HYDROCHLOROTHIAZIDE

NDC: 42658-141
Generic name: irbesartan and hydrochlorothiazide
Labeler / Manufacturer: Hisun Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20250101

FDA application: ANDA207896

## Active ingredients

- HYDROCHLOROTHIAZIDE: 12.5 mg/1
- IRBESARTAN: 150 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42658-141"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42658-141
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e6d11cd6-7204-4031-a6c5-8f6a33568ab4