# Losartan Potassium and Hydrochlorothiazide

NDC: 68788-8510
Generic name: Losartan Potassium and Hydrochlorothiazide
Labeler / Manufacturer: Preferred Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230822

FDA application: ANDA078245

## 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:"68788-8510"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68788-8510
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0f0c7234-b605-440f-abed-44f992d189a2