NDC 43602-421

Levothyroxine Sodium 0.1 mg tablet

On the label: Ascent 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

Strength

0.1 mg

Approval

ANDA ANDA215259

On the market since

Jan 18, 2023

Package NDCs

43602-421-10 43602-421-30 43602-421-90

Official label

DailyMed (National Library of Medicine), updated Jan 19, 2023

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