# Losartan Potassium and Hydrochlorothiazide

NDC: 62332-050
Generic name: Losartan Potassium and Hydrochlorothiazide
Labeler / Manufacturer: Alembic Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20160523

FDA application: ANDA091617

## 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:"62332-050"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62332-050
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=acecced9-2a61-435d-b7d4-b151cb7b7e5d