# Losartan potassium and Hydrochlorothiazide

NDC: 33342-052
Generic name: Losartan potassium and Hydrochlorothiazide
Labeler / Manufacturer: Macleods Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20120503

FDA application: ANDA202289

## 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:"33342-052"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=33342-052
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=a04b5622-2c49-4d61-92b1-5dc523af7a24