# Olmesartan Medoxomil and Hydrochlorothiazide

NDC: 50090-3701
Generic name: Olmesartan Medoxomil and Hydrochlorothiazide
Labeler / Manufacturer: A-S Medication Solutions
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20170424

FDA application: ANDA205391

## Active ingredients

- HYDROCHLOROTHIAZIDE: 12.5 mg/1
- OLMESARTAN MEDOXOMIL: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50090-3701"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-3701
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b78ad43f-f132-4f03-8c85-2cf9b3ab555b