# OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE

NDC: 70518-4577
Generic name: OLMESARTAN MEDOXOMIL AND HYDROCHLOROTHIAZIDE
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20260227

FDA application: ANDA207037

## Active ingredients

- HYDROCHLOROTHIAZIDE: 25 mg/1
- OLMESARTAN MEDOXOMIL: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-4577"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-4577
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9c68d45d-e4c8-4f6f-9ca5-faadc056e6e7