# Losartan Potassium and Hydrochlorothiazide

NDC: 50090-7199
Generic name: Losartan Potassium and Hydrochlorothiazide
Labeler / Manufacturer: A-S Medication Solutions
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20101006

FDA application: ANDA091629

## 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:"50090-7199"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-7199
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=98b97680-474c-4e70-89dd-15bb49773125