NDC 70710-1833

Levothyroxine Sodium 100 ug per 5 mL injection, powder, lyophilized, for solution

On the label: Zydus Pharmaceuticals (USA) Inc..

Where it's made

Zydus Lifesciences Limited

Vadodara, India · makes it and tests it

Serious problems, FDA action Last FDA inspection Apr 23, 2024. 2 inspections on record, 1 with serious problems.

Product details

Generic drug

Levothyroxine: see every company that makes it

Form

injection, powder, lyophilized, for solution, intravenous

Strength

100 ug per 5 mL

Approval

ANDA ANDA217066

On the market since

Nov 1, 2024

Package NDCs

70710-1833-1

Official label

DailyMed (National Library of Medicine), updated Sep 16, 2025

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