# OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE

NDC: 71335-2425
Generic name: olmesartan medoxomil and hydrochlorothiazide
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20170424

FDA application: ANDA207804

## 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:"71335-2425"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-2425
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=78eb9041-a738-4056-8705-8c1dd13a4da4