70436-116-82 (Image 01)
Leucovorin Calcium Injection, Powder, Lyophilized, For Solution
Product Images NDC 70436-116
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Product Visual Gallery
This gallery contains 5 technical images submitted to the FDA as part of the official labeling for Leucovorin Calcium (NDC 70436-116). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.
As provided by Slate Run Pharmaceuticals, 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.
Product Images & Figures Index
70436-117-80 (Image 02)
70436-118-80 (Image 03)
Leucovorin Calcium for Injection is a medication that is used intravenously or intramuscularly. Each vial contains 200 mg of Leucovorin Calcium, which is equivalent to 200 g of leucovorin. The solution should be reconstituted with sterile water for injection or bacteriostatic water for injection. It is important not to use a preservative-containing solution for doses greater than 10 mg. The usual dosage should be determined according to the package insert. The dry product and reconstituted solution should be stored at room temperature and protected from light. The container closure does not contain natural rubber latex. This product should not be used after the expiration date. It is distributed by Sate Run Pharmaceuticals in Ohio, USA.*
Structural Formula (Image 04)
70436-120-80 (Image 05)
This text is a description of Leucovorin Calcium for Injection, USP. Each vial contains 500 mg of Leucovorin Calcium. It is intended for intravenous or intramuscular use. The product is lyophilized and comes in a single-dose vial. Any unused portion should be discarded. The reconstituted solution contains 10 mg of Leucovorin Calcium per mL when mixed with sterile water or bacteriostatic water. It is advised not to use a preservative-containing solution for doses greater than 10 mg/m2. The usual dosage should be determined based on the package insert. The product should be stored at 20° to 25°C and protected from light. The container closure does not contain natural rubber latex. The lot was manufactured by Hainan Poly Phrm Co, Ltd in Haikou, Hairan Province, China and distributed by Slate Run Pharmaceuticals, LLC in Columbus, Ohio.*
* These product label images have been analyzed using experimental machine learning. Please verify findings with the primary label text.
