# OLMESARTAN MEDOXOMIL

NDC: 72303-0849
Generic name: Olmesartan medoxomil
Labeler / Manufacturer: HEC Pharm USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20260410

FDA application: ANDA211049

## Active ingredients

- OLMESARTAN MEDOXOMIL: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72303-0849"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72303-0849
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4f4d89ab-58c8-27ea-e063-6394a90a8723