# OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE

NDC: 50228-342
Generic name: OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE
Labeler / Manufacturer: ScieGen Pharmaceuticals Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20260519

FDA application: ANDA208465

## Active ingredients

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

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50228-342"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50228-342
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=52332190-2a12-d205-e063-6394a90ab7c5