# Losartan Potassium and Hydrochlorothiazide

NDC: 63629-2431
Generic name: losartan potassium and hydrochlorothiazide
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20121030

FDA application: ANDA201845

## 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:"63629-2431"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63629-2431
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0e015b9a-0ac1-4ec3-bbe7-7a672d30e1f4