NDC 67046-449

Losartan Potassium 100 mg tablet, film coated

On the label: Coupler Enterprises Inc.. It's a repackaged product: Coupler Enterprises Inc. rebottles it from Aurobindo Pharma Limited's NDC 65862-203.

Where the pills inside were made

Apl Healthcare Limited

Tirupati, India · makes it and tests it

Problems found, fixed voluntarily Last FDA inspection Dec 17, 2025. 5 inspections on record.

Aurobindo Pharma Limited

Medchal, India · makes it and tests it

Problems found, fixed voluntarily Last FDA inspection Jul 21, 2023. 13 inspections on record, 1 with serious problems.

Repackaging site

Product details

Generic drug
Losartan: see every company that makes it
Form
tablet, film coated
Strength
100 mg
Approval
ANDA ANDA090083
On the market since
Oct 6, 2010
Package NDCs
67046-449-30
Official label
DailyMed (National Library of Medicine), updated Dec 29, 2018

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