Levocarnitine Injection
Product Images NDC 0143-9852

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Levocarnitine (NDC 0143-9852). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Hikma Pharmaceuticals Usa Inc., these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

FDA Label Image

Structural Formula (Levocarnitine Injection Usp 1)

Chemical structure of Levocarnitine showing a quaternary ammonium group, hydroxyl group, and a carboxylate group arranged in a specific molecular configuration.*

FDA Label Image

Vial Label (Levocarnitine Injection Usp 2)

Levocarnitine Injection, USP 1 gram per 5 mL (200 mg/mL) intravenous injection single-dose vial label from Hikma Pharmaceuticals USA Inc. The label includes dosage strength, usage instructions, storage conditions, and barcodes, specifying use for intravenous administration only.*

FDA Label Image

Carton (Levocarnitine Injection Usp 3)

Levocarnitine Injection, USP 1 gram per 5 mL (200 mg/mL) intravenous injection. The label indicates it is for intravenous use only, supplied as 10 single-dose 5 mL vials. Manufactured by Hikma Farmaceutica (Portugal) and distributed by Hikma Pharmaceuticals USA Inc. Dosage instructions, storage conditions, and other regulatory information are also present.*

FDA Label Image

Representative Serialization Image (Levocarnitine Injection Usp 4)

A barcode label showing a QR code on the left and printed alphanumeric text on the right. The text includes identifiers such as a GTIN code, serial number, placeholder expiry date (EXP MMYYYY), and lot number (LOT ABCDE12345). There is no proprietary or drug name visible on this label.*

* About these descriptions: Image descriptions on this page are generated by automated AI analysis of the product label images from the manufacturer's FDA label submission (SPL). They are provided for reference only and may contain errors or omissions. Always rely on the printed label itself and the official FDA labeling, and consult a pharmacist or healthcare professional with any questions about this product.