NDC 72865-239

Levothyroxine Sodium 0.088 mg tablet

On the label: XLCare Pharmaceuticals, Inc..

Where it's made

Ascent Pharmaceuticals Inc

Central Islip, NY, United States · makes it, tests it and packages it

Problems found, fixed voluntarily Last FDA inspection Aug 9, 2024. 9 inspections on record.

Product details

Generic drug
Levothyroxine: see every company that makes it
Form
tablet, oral
Strength
0.088 mg
Approval
ANDA ANDA215259
On the market since
Jan 18, 2023
Package NDCs
72865-239-10 72865-239-90
Official label
DailyMed (National Library of Medicine), updated Feb 6, 2023

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