Levothyroxine Sodium 24201-0002

Product NDC

24201-0002

Manufacturer: Hikma Pharmaceuticals Usa Inc.
Dosage Form: Injection, Solution
Route: Intravenous
Product Type: Human Prescription Drug
Marketing Start: November 15, 2022
Listing Expires: December 31, 2026
Application: NDA214253

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Active Ingredients

Ingredient	Strength
Levothyroxine Sodium	100 ug/mL

Drug Class

Thyroxine [CS]l-Thyroxine [EPC]

Packaging Options(1)

24201-0002-01

1 VIAL, SINGLE-DOSE in 1 CARTON (24201-002-01) / 2 mL in 1 VIAL, SINGLE-DOSE

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