NDC 71205-949

Fenofibrate 160 mg tablet, film coated

On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Westminster Pharmaceuticals, LLC's NDC 69367-254.

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 Westminster Pharmaceuticals, LLC names for other drugs.

Repackaging site

Product details

Generic drug
Fenofibric Acid: every company that makes it
Form
tablet, film coated, oral
Strength
160 mg
Approval
ANDA ANDA207803
On the market since
Apr 23, 2020
Package NDCs
71205-949-30 71205-949-55 71205-949-60 71205-949-72 71205-949-78 71205-949-90
Official label
DailyMed (National Library of Medicine), updated Mar 1, 2022

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