NDC 71205-249

Valsartan and Hydrochlorothiazide 80 mg / 12.5 mg tablet, film coated

On the label: Proficient Rx LP. It's repackaged: Proficient Rx LP rebottles it from Lupin Pharmaceuticals, Inc.'s NDC 68180-103.

India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Lupin LimitedSalcette, IndiaMakes it and packages it Problems found, fixed voluntarilyNov 21, 2025 · 9 inspections, 1 with FDA action

Repackaging site

Product details

Generic drug
Hydrochlorothiazide and Valsartan: every company that makes it
Form
tablet, film coated, oral
Strength
80 mg / 12.5 mg
Approval
ANDA ANDA078946
On the market since
Mar 21, 2013
Package NDCs
71205-249-30 71205-249-60 71205-249-90
Official label
DailyMed (National Library of Medicine), updated Oct 1, 2019

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