# OLMESARTAN MEDOXOMIL

NDC: 42571-201
Generic name: olmesartan medoxomil
Labeler / Manufacturer: Micro Labs Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20200203

FDA application: ANDA206372

## Active ingredients

- OLMESARTAN MEDOXOMIL: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42571-201"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42571-201
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=de799a31-50ae-4b9e-a159-3d399b523dca