Levoleucovorin Calcium Injection, Solution
Product Images NDC 70121-1572

3 FDA label images from Amneal Pharmaceuticals Llc · 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 Levoleucovorin Calcium (NDC 70121-1572). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Amneal 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

FDA Label Image

1 (Levoleucovorin Injection Solution 10 mg 1)

1 (Levoleucovorin Injection Solution 10 mg 1)
Chemical structure of Levoleucovorin Calcium showing its molecular arrangement including amine, carboxylate, and calcium ion complex, with a note indicating hydration (nH2O where n = 3 to 6).*
FDA Label Image

1 (Levoleucovorin Injection Solution 10 mg 2)

1 (Levoleucovorin Injection Solution 10 mg 2)
Label for Levoleucovorin Injection 175 mg/17.5 mL (10 mg/mL) intravenous solution by Amneal Pharmaceuticals LLC. The label states it is a single-dose vial, with levoleucovorin calcium as the active ingredient. It includes dosage instructions, storage information, and manufacturing details from Amneal Pharmaceuticals Pvt. Ltd., India.*
FDA Label Image

1 (Levoleucovorin Injection Solution 10 mg 3)

1 (Levoleucovorin Injection Solution 10 mg 3)
Levoleucovorin Injection 175 mg/17.5 mL (10 mg/mL) single-dose vial label by Amneal Pharmaceuticals LLC. The label states the vial contains 10.0 mg levoleucovorin calcium equivalent to 10 mg levoleucovorin per mL, and is for intravenous use only. Storage instructions indicate refrigeration at 2° to 8°C (36° to 46°F) and protection from light until contents are used.*

* 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.