NDC 71205-291

Bupropion HydrochlorideXL 150 mg tablet, extended release

On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Epic Pharma, LLC's NDC 42806-348.

China: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
CSPC Ouyi Pharmaceutical Co., Ltd.Shijiazhuang, ChinaMakes it Problems found, fixed voluntarilySep 5, 2024 · 8 inspections

Repackaging site

Product details

Generic drug
Bupropion: every company that makes it
Form
tablet, extended release, oral
Strength
150 mg
Approval
ANDA ANDA207224
On the market since
Oct 1, 2017
Package NDCs
71205-291-30 71205-291-60 71205-291-90
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?