# OLMESARTAN MEDOXOMIL, AMLODIPINE and HYDROCHLOROTHIAZIDE

NDC: 42571-246
Generic name: Olmesartan Medoxomil, Amlodipine besylate and Hydrochlorothiazide
Labeler / Manufacturer: Micro Labs Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET, FILM COATED
Routes: ORAL
Marketing started: 20260301

FDA application: ANDA207437

## 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:"42571-246"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42571-246
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9fb71df8-f70f-47dc-9465-8d8748261caf