NDC 50090-4329
Olmesartan Medoxomil and Hydrochlorothiazide 20 mg / 12.5 mg tablet, film coated
On the label: A-S Medication Solutions. It's repackaged from NDC 57664-758, made by Sun Pharmaceutical Industries, Inc. (Olmesartan Medoxomil 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 and relabels 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 A-S Medication Solutions names for other drugs.
Product details
- Generic drug
- Hydrochlorothiazide and Olmesartan: every company that makes it
- Form
- tablet, film coated
- Strength
- 20 mg / 12.5 mg
- Approval
- NDA NDA021532
- On the market since
- Oct 26, 2016
- Package NDCs
50090-4329-050090-4329-1- Official label
- DailyMed (National Library of Medicine), updated Jun 13, 2019
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?