NDC 51655-467
Hydroxyzine Hydrochloride 50 mg tablet, film coated
On the label: Northwind Pharmaceuticals. It's repackaged: Northwind Pharmaceuticals rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0093-5062.
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
- Northwind Health Company, LLC, Indianapolis, IN, United States · repackages it
Product details
- Generic drug
- Hydroxyzine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA088619
- On the market since
- Oct 29, 2020
- Package NDCs
51655-467-52- Official label
- DailyMed (National Library of Medicine), updated Jan 1, 2026
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