# Olmesartan medoxomil Amlodipine and Hydrochlorothiazide

NDC: 33342-244
Generic name: Olmesartan medoxomil Amlodipine and Hydrochlorothiazide
Labeler / Manufacturer: Macleods Pharmaceuticals Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20250718

FDA application: ANDA207088

## 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:"33342-244"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=33342-244
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=52c013e1-8c31-4bed-9241-e7845873ebe8