Levocarnitine Injection, Solution
Product Images NDC 36000-368

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Levocarnitine (NDC 36000-368). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Baxter Healthcare Corporation, 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

Carton-3.jpg (Carton 3 01)

Packaging label for Levocarnitine Injection, USP, 1 g/5 mL (200 mg/mL) solution for intravenous use, manufactured by Baxter Pharmaceuticals India Pvt Ltd and labeled for Baxter Healthcare Corporation. The label includes usage instructions, storage conditions, barcode, lot number, expiration date, and a note to discard unused portions. The package contains 10 single-dose vials of 5 mL each.*

FDA Label Image

Carton-4.jpg (Carton 3)

Carton label for Levocarnitine Injection, USP 1 g/5 mL (200 mg/mL) solution for intravenous use. The label indicates it contains 10 single-dose vials of 5 mL each and is labeled by Baxter Healthcare Corporation. The NDC number 36000-368-10 and caution for intravenous use and discarding unused portions are also displayed.*

FDA Label Image

Container-2.jpg (Container 2)

Label for Levocarnitine Injection, USP 1 g/5 mL (200 mg/mL) single-dose vial for intravenous use. The label includes storage instructions, manufacturer details as Baxter Healthcare Corporation, and NDC 36000-368-01.*

FDA Label Image

Description-1.jpg (Description 1)

Chemical structure diagram of levocarnitine, showing its molecular arrangement with functional groups including hydroxyl, carboxylate, and a trimethylammonium group.*

* 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.