Leucovorin Calcium Injection, Powder, Lyophilized, For Solution
Product Images NDC 68083-668

3 FDA label images from Gland Pharma Limited · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 3 technical images submitted to the FDA as part of the official labeling for Leucovorin Calcium (NDC 68083-668). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Gland Pharma Limited, these visuals offer a comprehensive scientific overview of the product's physical and chemical identity, aiding pharmacists and researchers in product verification and study.

Product Images & Figures Index

FDA Label Image

Leucovorin-spl-structure (Leucovorin Spl Structure)

Leucovorin-spl-structure (Leucovorin Spl Structure)
Chemical structure of Leucovorin Calcium, showing its molecular framework with labeled atoms and bonds, including calcium coordination.*
FDA Label Image

Leucovorin-spl-carton-label (Leucovorin Spl Container Label)

Leucovorin-spl-carton-label (Leucovorin Spl Container Label)
Leucovorin Calcium injection, USP, lyophilized powder for solution, 500 mg per vial, for intravenous or intramuscular use. The label includes NDC 68083-668 and manufacturer information for Gland Pharma Limited, Hyderabad, India. It notes reconstitution instructions and storage conditions, and the vial does not contain natural rubber latex closure.*
FDA Label Image

Leucovorin-spl-carton-label (Leucovorin Spl Carton Label)

Leucovorin-spl-carton-label (Leucovorin Spl Carton Label)
Packaging label for Leucovorin Calcium 500 mg per vial injection, USP, lyophilized powder for solution. The label indicates it is for intravenous or intramuscular use, Rx only, with NDC 68083-668-01. Manufactured by Gland Pharma Limited, Hyderabad, India. The label includes usage instructions and storage conditions.*

* 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.