NDC 42291-924
olmesartan medoxomil-hydrochlorothiazide 20 mg / 12.5 mg tablet, film coated
On the label: AvKARE, Inc.. It's repackaged: AvKARE, Inc. rebottles it from Cosette Pharmaceuticals, Inc.'s NDC 0713-0863.
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 Cosette Pharmaceuticals, Inc. names for other drugs.
Product details
- Generic drug
- Hydrochlorothiazide and Olmesartan: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 20 mg / 12.5 mg
- Approval
- NDA NDA021532
- On the market since
- Jul 27, 2023
- Package NDCs
42291-924-90- Official label
- DailyMed (National Library of Medicine), updated Jan 19, 2026
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