# Losartan Potassium and Hydrochlorothiazide

NDC: 70518-3420
Generic name: losartan potassium and hydrochlorothiazide
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20220516

FDA application: ANDA204901

## Active ingredients

- HYDROCHLOROTHIAZIDE: 25 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:"70518-3420"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-3420
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=446e6998-01f6-4de0-be57-7fecf5448e95