Leucovorin Calcium Injection, Powder, Lyophilized, For Suspension
Product Images NDC 67457-530

4 FDA label images from Mylan Institutional Llc · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Leucovorin Calcium (NDC 67457-530). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Mylan Institutional Llc, 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

Structure (Image 01)

Structure (Image 01)
Chemical structure diagram of leucovorin calcium showing its molecular connectivity including a pteridine ring system, a benzoyl group, and a calcium salt of a carboxylic acid moiety.*
FDA Label Image

Carton 100 mg (Image 02)

Carton 100 mg (Image 02)
Packaging label for Leucovorin Calcium injection powder, lyophilized for suspension, 100 mg per vial. The label specifies its use for intravenous or intramuscular administration and indicates the product must be diluted before use. Manufactured by Mylan Institutional LLC, the label includes storage instructions and dosage warnings. It features the NDC 67457-528-10 and displays the Mylan logo.*
FDA Label Image

Carton 200 mg (Image 03)

Carton 200 mg (Image 03)
Packaging label for Leucovorin Calcium injection, powder, lyophilized for suspension, 200 mg per vial. The label indicates it is for intravenous or intramuscular use, must be diluted, and is a single-dose vial. Manufactured by Mylan Institutional LLC. The label includes usage instructions and storage information.*
FDA Label Image

300 mg Carton (Image 04)

300 mg Carton (Image 04)
Packaging label for Leucovorin Calcium injection, lyophilized powder for suspension, 350 mg per vial. The product is for intravenous or intramuscular use, must be diluted, and is single-dose. Manufactured for Mylan Institutional LLC, Rockford, IL, and made in India. The label includes usage instructions, storage conditions, and warning notes about preservatives.*

* 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.