NDC 67046-274
Hydrochlorothiazide 50 mg tablet
On the label: Coupler Enterprises Inc.. It's repackaged: Coupler Enterprises Inc. rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0172-2089.
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 Teva Pharmaceuticals USA, Inc. names for other drugs.
Product details
- Generic drug
- Hydrochlorothiazide: every company that makes it
- Form
- tablet
- Strength
- 50 mg
- Approval
- ANDA ANDA083177
- On the market since
- Mar 9, 2010
- Package NDCs
67046-274-30- Official label
- DailyMed (National Library of Medicine), updated Mar 9, 2010
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