NDC 53808-1120
Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide 5 mg / 20 mg / 12.5 mg tablet, film coated
On the label: State of Florida DOH Central Pharmacy. It's repackaged from NDC 57664-796, made by Sun Pharmaceutical Industries, Inc. (Olmesartan Medoxomil, Amlodipine and Hydrochlorothiazide). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that repackages it). 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 State of Florida DOH Central Pharmacy names for other drugs.
Product details
- Generic drug
- Amlodipine and Hydrochlorothiazide and Olmesartan: every company that makes it
- Form
- tablet, film coated
- Strength
- 5 mg / 20 mg / 12.5 mg
- Approval
- NDA NDA200175
- On the market since
- Oct 25, 2018
- Package NDCs
53808-1120-1- Official label
- DailyMed (National Library of Medicine), updated Jan 21, 2019
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