NDC 70518-4402

Levothyroxine sodium 125 ug tablet

On the label: Remedyrepack Inc.. It's a repackaged product: Remedyrepack Inc. rebottles it from Accord Healthcare Inc.'s NDC 16729-453.

Where the pills inside were made

Excella GmbH & Co. KG

Feucht, Germany · makes the active ingredient

Problems found, fixed voluntarily Last FDA inspection Oct 19, 2022. 7 inspections on record.

Intas Pharmaceuticals Limited

Dehradun, India · makes it and tests it

Serious problems, FDA action Last FDA inspection Sep 16, 2025. 1 inspection on record, 1 with serious problems.

Recalls

Product details

Generic drug
Levothyroxine: see every company that makes it
Form
tablet, oral
Strength
125 ug
Approval
ANDA ANDA212399
On the market since
Jul 24, 2025
Package NDCs
70518-4402-0
Official label
DailyMed (National Library of Medicine), updated Sep 10, 2026

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