NDC 17856-0150
Hydroxyzine Hydrochloride 10 mg per 5 mL syrup
On the label: Atlantic Biologicals Corps.. It's repackaged: Atlantic Biologicals Corps. rebottles it from Morton Grove Pharmaceuticals, Inc.'s NDC 60432-150.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Morton Grove Pharmaceuticals, Inc. | Morton Grove, Illinois, United States | Makes it, tests it, packages it and labels it | Serious problems, FDA actionFeb 5, 2016 · 6 inspections, 1 with FDA action |
Repackaging site
- Atlantic Biologicals Corps, Location not on file · repackages it and relabels it
Recalls
- Dec 9, 2020 · Class II · Morton Grove Pharmaceuticals, Inc.
Failed Impurities/Degradation Specification: OOS for the following - unknown degradant/impurity, 4-chorobenzophenone, and for total impurities.
Lots: Lot#: a) UU1328, Exp 10/21; b) UU1207, Exp 07/21; UU1326, Exp 09/21; UU1327, Exp 10/21.
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Hydroxyzine: every company that makes it
- Form
- syrup
- Strength
- 10 mg per 5 mL
- Approval
- ANDA ANDA087294
- On the market since
- Mar 9, 1995
- Package NDCs
17856-0150-1- Official label
- DailyMed (National Library of Medicine), updated Jan 27, 2021
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