Drugplain

NDC 63323-649-07

Levothyroxine Sodium 100 ug/5mL

LEVOTHYROXINE SODIUM ANHYDROUS · INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

No Recall History

Levothyroxine Sodium is a injection, powder, lyophilized, for solution containing levothyroxine sodium anhydrous at a strength of 100 ug/5mL. Manufactured by Fresenius Kabi USA, LLC.

Key Facts

Brand Name
Levothyroxine Sodium
Generic Name
LEVOTHYROXINE SODIUM ANHYDROUS
NDC Code (Package)
63323-649-07
NDC Code (Product)
63323-649
Manufacturer
Fresenius Kabi USA, LLC
Strength
100 ug/5mL
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAVENOUS
Marketing Status
Application #
NDA202231
Marketing Start
06/24/2011

Recall History

No Recall History

Not medical advice. This information is for reference only. Always consult your doctor or pharmacist.