NDC 64205-820
Hydrochlorothiazide 25 mg tablet
On the label: ReadyMeds. It's repackaged from NDC 67253-820, made by DAVA Pharmaceuticals, Inc. (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 ReadyMeds names for other drugs.
Product details
- Generic drug
- Hydrochlorothiazide: every company that makes it
- Form
- tablet
- Strength
- 25 mg
- Approval
- ANDA ANDA087059
- On the market since
- Nov 5, 1980
- Package NDCs
64205-820-30- Official label
- DailyMed (National Library of Medicine), updated Jun 20, 2014
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?