NDC 71205-083

Hydroxyzine Hydrochloride 50 mg tablet, film coated

On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Teva Pharmaceuticals USA, Inc.'s NDC 0093-5062.

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 Teva Pharmaceuticals USA, Inc. names for other drugs.

Repackaging site

Product details

Generic drug
Hydroxyzine: every company that makes it
Form
tablet, film coated, oral
Strength
50 mg
Approval
ANDA ANDA088619
On the market since
Oct 22, 2012
Package NDCs
71205-083-15 71205-083-20 71205-083-30 71205-083-60 71205-083-90
Official label
DailyMed (National Library of Medicine), updated Nov 1, 2022

Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?