NDC 0517-1045 – Levocarnitine

Levocarnitine 200 mg/mL · Injection, Solution · Intravenous

Human Prescription Drug 1 recall

Product NDC0517-1045

Product details

Brand name
Levocarnitine
Generic name
Levocarnitine
Labeler
American Regent, Inc.
Dosage form
Injection, Solution
Route
Intravenous
Marketing category
ANDA · ANDA075861
Marketed since
June 21, 2023
Listing expires
December 31, 2026
Pharmacologic class
Carnitine Analog

Active ingredients

Uses, dosage, side effects and warnings for Levocarnitine →

Package NDC codes (1)

Package NDCDescriptionSince
0517-1045-055 VIAL, SINGLE-DOSE in 1 CARTON (0517-1045-05) / 5 mL in 1 VIAL, SINGLE-DOSE (0517-1045-01)Jun 21, 2023

Recalls mentioning this NDC

Other Levocarnitine products