Leucovorin Calcium Injection, Powder, Lyophilized, For Solution
Product Images NDC 63323-711

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 6 technical images submitted to the FDA as part of the official labeling for Leucovorin Calcium (NDC 63323-711). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Fresenius Kabi Usa, 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

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Chemical structure diagram of Leucovorin Calcium, showing its molecular arrangement including amino groups, rings, and calcium ion complex.*
FDA Label Image

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FDA Label Image

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Label for Leucovorin Calcium injection powder for solution, 200 mg per vial, intended for intravenous or intramuscular use. The label states it contains leucovorin calcium equivalent to 200 mg leucovorin base and sodium chloride. It includes storage instructions and cautions about preservative use. Labeler is Fresenius Kabi.*
FDA Label Image

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Packaging label for Leucovorin Calcium for Injection, 200 mg per vial, a lyophilized powder for solution by Fresenius Kabi USA, LLC. The label includes instructions for reconstitution and notes that it is for intravenous or intramuscular use. The label also includes storage information, manufacturer details, and a barcode.*
FDA Label Image

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Label for Leucovorin Calcium for Injection, 500 mg per vial, by Fresenius Kabi USA, LLC. The label states the product is a lyophilized powder for injection for intravenous or intramuscular use. It includes information on vial contents, storage conditions, and handling instructions. The NDC number 63323-711-00 and a barcode are also visible.*
FDA Label Image

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Leucovorin Calcium 500 mg per vial injection, lyophilized powder for solution. The packaging label details the product for intravenous or intramuscular use, with instructions for reconstitution and storage. The labeler is Fresenius Kabi USA, LLC, and it includes a barcode and NDC number 63323-711-00.*

* 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.