NDC 11534-206
Hydroxyzine Hydrochloride 50 mg tablet, film coated
On the label: Sunrise Pharmaceutical, 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 Sunrise Pharmaceutical, Inc. names for other drugs.
Product details
- Generic drug
- Hydroxyzine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA207121
- On the market since
- May 1, 2024
- Package NDCs
11534-206-0111534-206-0311534-206-04- Official label
- DailyMed (National Library of Medicine), updated Dec 9, 2024
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?