# Losartan Potassium and Hydrochlorothiazide

NDC: 43063-986
Generic name: Losartan Potassium and Hydrochlorothiazide
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
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: 12.5 mg/1
- LOSARTAN POTASSIUM: 50 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"43063-986"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=43063-986
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=dcb39c6b-430d-4b3d-ba6f-5bf1efe116aa