# OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE

NDC: 72603-291
Generic name: OLMESARTAN MEDOXOMIL and HYDROCHLOROTHIAZIDE
Labeler / Manufacturer: NorthStar RxLLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20240408

FDA application: ANDA204801

## Active ingredients

- 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:"72603-291"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72603-291
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=364af4fe-cde8-466f-b56f-d93d532b56f5