# Valsartan and Hydrochlorothiazide

NDC: 51655-243
Generic name: valsartan and hydrochlorothiazide
Labeler / Manufacturer: Northwind Health Company, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20221116

FDA application: ANDA078020

## Active ingredients

- HYDROCHLOROTHIAZIDE: 25 mg/1
- VALSARTAN: 320 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51655-243"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51655-243
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f2b749a6-17ff-e044-e053-2995a90aea28