NDC 51655-079
Hydroxyzine Hydrochloride 25 mg tablet, film coated
On the label: Northwind Pharmaceuticals. It's repackaged from NDC 23155-106, made by Heritage Pharmaceuticals Inc. (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 Northwind Pharmaceuticals names for other drugs.
Product details
- Generic drug
- Hydroxyzine: every company that makes it
- Form
- tablet, film coated
- Strength
- 25 mg
- Approval
- ANDA ANDA040804
- On the market since
- Feb 26, 2015
- Package NDCs
51655-079-25- Official label
- DailyMed (National Library of Medicine), updated Apr 1, 2015
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?