# Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide

NDC: 0093-5006
Generic name: Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide
Labeler / Manufacturer: Teva Pharmaceuticals USA, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20161114

FDA application: ANDA202491

## Active ingredients

- AMLODIPINE BESYLATE: 5 mg/1
- HYDROCHLOROTHIAZIDE: 12.5 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:"0093-5006"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0093-5006
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5c128ef2-60a6-40f3-b37f-ee139fe27987