NDC 25021-469 – Levothyroxine Sodium

Levothyroxine Sodium Anhydrous 200 ug/5mL · Injection, Powder, Lyophilized, For Solution · Intravenous

Human Prescription Drug

Product NDC25021-469

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

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

Package NDC codes (1)

Package NDCDescriptionSince
25021-469-101 VIAL in 1 CARTON (25021-469-10) / 5 mL in 1 VIALJan 1, 2024

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