NDC 25021-470 – Levothyroxine Sodium

Levothyroxine Sodium Anhydrous 500 ug/5mL · Injection, Powder, Lyophilized, For Solution · Intravenous

Human Prescription Drug

Product NDC25021-470

Product details

Brand name: Levothyroxine Sodium
Generic name: Levothyroxine Sodium Anhydrous
Labeler: Sagent Pharmaceuticals
Dosage form: Injection, Powder, Lyophilized, For Solution
Route: Intravenous
Marketing category: ANDA · ANDA208749
Marketed since: January 1, 2024
Listing expires: December 31, 2026
Pharmacologic class: l-Thyroxine

Active ingredients

Levothyroxine Sodium Anhydrous 500 ug/5mL

Uses, dosage, side effects and warnings for Levothyroxine Sodium →

Package NDC codes (1)

Package NDC	Description	Since
25021-470-10	1 VIAL in 1 CARTON (25021-470-10) / 5 mL in 1 VIAL	Jan 1, 2024

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