NDC 72603-667

Levothyroxine Sodium 137 ug tablet

On the label: Northstar Rx LLC..

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

Product details

Generic drug
Levothyroxine: every company that makes it
Form
tablet, oral
Strength
137 ug
Approval
ANDA ANDA211417
On the market since
Apr 8, 2025
Package NDCs
72603-667-01 72603-667-02 72603-667-10 72603-667-11
Official label
DailyMed (National Library of Medicine), updated Aug 20, 2026

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