NDC 71205-751
Hydrochlorothiazide 50 mg tablet
On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP 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.
Repackaging site
- Proficient Rx LP, Thousand Oaks, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Hydrochlorothiazide: every company that makes it
- Form
- tablet, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA083177
- On the market since
- Jan 7, 1980
- Package NDCs
71205-751-3071205-751-6071205-751-90- Official label
- DailyMed (National Library of Medicine), updated Feb 1, 2023
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?