NDC 72789-512
Hydrochlorothiazide 25 mg tablet
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0172-2083.
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.
Repackaging site
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
Product details
- Generic drug
- Hydrochlorothiazide: every company that makes it
- Form
- tablet, oral
- Strength
- 25 mg
- Approval
- ANDA ANDA083177
- On the market since
- Jan 12, 1973
- Package NDCs
72789-512-3072789-512-6072789-512-90- Official label
- DailyMed (National Library of Medicine), updated Nov 4, 2026
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