# Olmesartan Medoxomil and Hydrochlorothiazide

NDC: 70518-2269
Generic name: Olmesartan Medoxomil and Hydrochlorothiazide
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20190816

FDA application: ANDA204233

## Active ingredients

- HYDROCHLOROTHIAZIDE: 12.5 mg/1
- OLMESARTAN MEDOXOMIL: 40 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-2269"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-2269
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=de815d64-b8d4-46a8-95b8-c230abe7f767