NDC 68180-217

Losartan Potassium and Hydrochlorothiazide 25 mg / 100 mg tablet

On the label: Lupin Pharmaceuticals, Inc..

India: 2

Where it's made

FactoryWhereRoleLast FDA inspection
Lupin LimitedSalcette, IndiaMakes it and packages it Problems found, fixed voluntarilyNov 21, 2025 · 9 inspections, 1 with FDA action
Lupin LimitedPithampur, IndiaMakes it and packages it Serious problems, FDA actionJul 17, 2025 · 6 inspections, 4 with FDA action

Recalls

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug
Hydrochlorothiazide and Losartan: every company that makes it
Form
tablet, oral
Strength
25 mg / 100 mg
Approval
ANDA ANDA078245
On the market since
Oct 6, 2010
Package NDCs
68180-217-01 68180-217-03 68180-217-06 68180-217-09
Official label
DailyMed (National Library of Medicine), updated Jul 16, 2026

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