NDC 53808-0632
Hydroxyzine Hydrochloride 50 mg tablet, film coated
On the label: State of Florida DOH Central Pharmacy. It's repackaged from NDC 68462-362, made by Glenmark Generics Inc., USA (Hydroxyzine Hydrochloride). That product's FDA listing has since ended, so its label and factories are no longer published.
Where the pills inside were made
This label doesn't name the factory that makes the drug (it lists 1 site that repackages it). 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 State of Florida DOH Central Pharmacy names for other drugs.
Product details
- Generic drug
- Hydroxyzine: every company that makes it
- Form
- tablet, film coated
- Strength
- 50 mg
- Approval
- ANDA ANDA040812
- On the market since
- Jan 1, 2013
- Package NDCs
53808-0632-1- Official label
- DailyMed (National Library of Medicine), updated Sep 11, 2013
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