# Valsartan and Hydrochlorothiazide

NDC: 71205-042
Generic name: Valsartan and Hydrochlorothiazide
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20160520

FDA application: ANDA201662

## Active ingredients

- HYDROCHLOROTHIAZIDE: 12.5 mg/1
- VALSARTAN: 320 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71205-042"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71205-042
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ec24af8d-29a3-4217-8f06-ac217ea55b9e