NDC 33342-399

Levothyroxine Sodium 125 ug tablet

On the label: Macleods Pharmaceuticals Limited.

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Macleods Pharmaceuticals LimitedValsad, IndiaMakes it, makes the active ingredient, tests it, packages it, labels it and mills it Problems found, fixed voluntarilyAug 4, 2026 · 5 inspections

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
125 ug
Approval
ANDA ANDA211417
On the market since
Dec 21, 2022
Package NDCs
33342-399-10 33342-399-11 33342-399-44
Official label
DailyMed (National Library of Medicine), updated Mar 4, 2024

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