NDC 72789-272

Levothyroxine sodium 50 ug tablet

On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Accord Healthcare Inc.'s NDC 16729-448.

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, oral
Strength
50 ug
Approval
ANDA ANDA212399
On the market since
Nov 25, 2020
Package NDCs
72789-272-30 72789-272-90
Official label
DailyMed (National Library of Medicine), updated Feb 25, 2026

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