# Losartan Potassium and Hydrochlorothiazide

NDC: 42708-193
Generic name: losartan potassium and hydrochlorothiazide
Labeler / Manufacturer: QPharma, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20180215

FDA application: ANDA204901

## Active ingredients

- HYDROCHLOROTHIAZIDE: 12.5 mg/1
- LOSARTAN POTASSIUM: 50 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42708-193"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42708-193
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=499208e5-21ab-d4fe-e063-6294a90a9a78