# OLMESARTAN MEDOXOMIL and HYDROCHOLOROTHIAZIDE

NDC: 42571-206
Generic name: Olmesartan medoxomil and hydrocholorothiazide
Labeler / Manufacturer: Micro Labs Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20261015

FDA application: ANDA206371

## Active ingredients

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

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42571-206"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42571-206