NDC 54838-502
Hydroxyzine Hydrochloride 10 mg per 5 mL solution
On the label: Lannett Company, Inc..
Where it's 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 Lannett Company, Inc. names for other drugs.
Recalls
- Oct 11, 2018 · Class II · Lannett Company, Inc.
CGMP Deviations: cleaning procedures during manufacturing caused out of specification results for unknown impurities.
Lots: Lot #: 1097, Exp 10/18
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
- solution, oral
- Strength
- 10 mg per 5 mL
- Approval
- ANDA ANDA201674
- On the market since
- Aug 21, 2013
- Package NDCs
54838-502-80- Official label
- DailyMed (National Library of Medicine), updated Jan 24, 2023
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