NDC 63323-649 – Levothyroxine Sodium

Levothyroxine Sodium Anhydrous 100 ug/5mL · Injection, Powder, Lyophilized, For Solution · Intravenous

Human Prescription Drug

Product NDC63323-649

Product details

Brand name
Levothyroxine Sodium
Generic name
Levothyroxine Sodium Anhydrous
Labeler
Fresenius Kabi USA, LLC
Dosage form
Injection, Powder, Lyophilized, For Solution
Route
Intravenous
Marketing category
NDA · NDA202231
Marketed since
June 24, 2011
Listing expires
December 31, 2026
Pharmacologic class
l-Thyroxine

Active ingredients

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

Package NDC codes (3)

Package NDCDescriptionSince
63323-649-071 VIAL, SINGLE-DOSE in 1 CARTON (63323-649-07) / 5 mL in 1 VIAL, SINGLE-DOSEJun 24, 2011
63323-649-161 VIAL, SINGLE-DOSE in 1 CARTON (63323-649-16) / 5 mL in 1 VIAL, SINGLE-DOSEJun 24, 2011
63323-649-941 VIAL, SINGLE-DOSE in 1 CARTON (63323-649-94) / 5 mL in 1 VIAL, SINGLE-DOSEJun 24, 2011

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