NDC 17856-0507
Hydroxyzine Hydrochloride 10 mg per 5 mL solution
On the label: Atlantic Biologicals Corps.. It's repackaged: Atlantic Biologicals Corps. rebottles it from Lannett Company, Inc.'s NDC 54838-502.
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 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
17856-0507-117856-0507-2- Official label
- DailyMed (National Library of Medicine), updated May 12, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?