# LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE

NDC: 31722-756
Generic name: LOSARTAN POTASSIUM AND HYDROCHLOROTHIAZIDE
Labeler / Manufacturer: Camber Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20260527

FDA application: ANDA219869

## Active ingredients

- LOSARTAN POTASSIUM: 100 mg/1
- HYDROCHLOROTHIAZIDE: 12.5 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"31722-756"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=31722-756
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=cdf59426-2a2f-4a60-943a-e6cef3eb31e1