NDC 70934-234
Hydroxyzine Hydrochloride 25 mg tablet, film coated
On the label: Denton Pharma, Inc. DBA Northwind Pharmaceuticals.. It's repackaged: Denton Pharma, Inc. DBA Northwind Pharmaceuticals. rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0093-5061.
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
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals, Location not on file · repackages it
Product details
- Generic drug
- Hydroxyzine: every company that makes it
- Form
- tablet, film coated
- Strength
- 25 mg
- Approval
- ANDA ANDA088618
- On the market since
- Aug 2, 2019
- Package NDCs
70934-234-1070934-234-30- Official label
- DailyMed (National Library of Medicine), updated Sep 21, 2020
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