NDC 70518-4165
olmesartan medoxomil / amlodipine besylate / hydrochlorothiazide 5 mg / 25 mg / 40 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Par Health USA, LLC's NDC 49884-788.
Where the pills inside were 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 / 25 mg / 40 mg
- Approval
- ANDA ANDA206137
- On the market since
- Aug 22, 2024
- Package NDCs
70518-4165-0- Official label
- DailyMed (National Library of Medicine), updated Oct 19, 2026
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