NDC 68180-965

Levothyroxine Sodium 0.025 mg tablet

On the label: Lupin Pharmaceuticals, Inc..

India: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Lupin LimitedDhar, IndiaMakes it and packages it Problems found, fixed voluntarilySep 27, 2024 · 4 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
0.025 mg
Approval
ANDA ANDA209713
On the market since
Mar 20, 2019
Package NDCs
68180-965-01 68180-965-02 68180-965-03 68180-965-09
Official label
DailyMed (National Library of Medicine), updated Mar 19, 2025

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