NDC 72865-236

Levothyroxine Sodium 0.025 mg tablet

On the label: XLCare Pharmaceuticals, Inc..

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Ascent Pharmaceuticals IncCentral Islip, NY, United StatesMakes it, tests it and packages it Problems found, fixed voluntarilyAug 9, 2024 · 9 inspections

Product details

Generic drug
Levothyroxine: every company that makes it
Form
tablet, oral
Strength
0.025 mg
Approval
ANDA ANDA215259
On the market since
Jan 18, 2023
Package NDCs
72865-236-10 72865-236-90
Official label
DailyMed (National Library of Medicine), updated Feb 6, 2023

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