NDC 49884-787

olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide 5 mg / 40 mg / 12.5 mg tablet, film coated

On the label: Par Health USA, LLC.

Where it's made

This label doesn't name the factory that makes the drug. Companies don't have to print it on the label. The maker's name is often on the stock bottle your pharmacy used; you can ask the pharmacist. See the plants Par Health USA, LLC names for other drugs.

Product details

Generic drug
Amlodipine and Hydrochlorothiazide and Olmesartan: every company that makes it
Form
tablet, film coated, oral
Strength
5 mg / 40 mg / 12.5 mg
Approval
ANDA ANDA206137
On the market since
Oct 26, 2016
Package NDCs
49884-787-09 49884-787-11
Official label
DailyMed (National Library of Medicine), updated Sep 11, 2026

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