NDC 67296-0055
Hydroxyzine Hydrochloride 25 mg tablet, film coated
On the label: RedPharm Drug Inc.. It's repackaged from NDC 5011-308, which isn't on any FDA listing we can find.
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 RedPharm Drug Inc. names for other drugs.
Product details
- Generic drug
- Hydroxyzine: every company that makes it
- Form
- tablet, film coated
- Strength
- 25 mg
- Approval
- ANDA ANDA088618
- On the market since
- Dec 7, 2010
- Package NDCs
67296-0055-2- Official label
- DailyMed (National Library of Medicine), updated Jul 14, 2011
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?