NDC 70934-901

Levothyroxine sodium 175 ug tablet

On the label: Denton Pharma, Inc. DBA Northwind Pharmaceuticals.. It's repackaged: Denton Pharma, Inc. DBA Northwind Pharmaceuticals. rebottles it from Accord Healthcare Inc.'s NDC 16729-456.

Germany: 1India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Excella GmbH & Co. KGFeucht, GermanyMakes the active ingredient Problems found, fixed voluntarilyOct 19, 2022 · 7 inspections
Intas Pharmaceuticals LimitedDehradun, IndiaMakes it and tests it Serious problems, FDA actionSep 16, 2025 · 1 inspection, 1 with FDA action

Repackaging site

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
Levothyroxine: every company that makes it
Form
tablet
Strength
175 ug
Approval
ANDA ANDA212399
On the market since
Dec 27, 2021
Package NDCs
70934-901-30
Official label
DailyMed (National Library of Medicine), updated Dec 28, 2021

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