# LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE

NDC: 72189-098
Generic name: LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE
Labeler / Manufacturer: Direct_Rx
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200612

FDA application: ANDA077157

## Active ingredients

- HYDROCHLOROTHIAZIDE: 12.5 mg/1
- LOSARTAN POTASSIUM: 100 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72189-098"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72189-098
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=8de04bf2-83dd-c494-e053-2a95a90abade