NDC 51655-422
Hydrochlorothiazide 50 mg tablet
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Unichem Pharmaceuticals (USA), Inc.'s NDC 29300-129.
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 Unichem Pharmaceuticals (USA), Inc. names for other drugs.
Repackaging site
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Recalls
- Jul 30, 2015 · Class II · Unichem Pharmaceuticals Usa Inc
Presence of Foreign Tablet: A pharmacist found a clopidogrel tablet in the 1000-count bottle of hydrochlorothiazide 25 mg tablets.
Lots: Lot #: GHYL15028, Exp April 2018
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Hydrochlorothiazide: every company that makes it
- Form
- tablet, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA040907
- On the market since
- Dec 29, 2022
- Package NDCs
51655-422-2651655-422-52- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2026
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