Leucovorin Calcium Injection, Powder, Lyophilized, For Solution
Product Images NDC 68001-648

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Leucovorin Calcium (NDC 68001-648). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Bluepoint Laboratories, 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

Carton (Leucovorin Calcium for Injection USP 100mg per vial)

Carton (Leucovorin Calcium for Injection USP 100mg per vial)
Packaging label for Leucovorin Calcium injection, 100 mg per vial, lyophilized powder for solution. The label indicates it is for intravenous or intramuscular use and contains one single-dose vial. Manufactured for BluePoint Laboratories, the label includes NDC 68001-648-36 and instructions referencing reconstitution and storage conditions.*
FDA Label Image

Carton (Leucovorin Calcium for Injection USP 200mg per vial)

Carton (Leucovorin Calcium for Injection USP 200mg per vial)
Packaging label for Leucovorin calcium 200 mg per vial injection, lyophilized powder for intravenous or intramuscular use. The label includes directions to reconstitute, storage instructions, and manufacturer information for BluePoint Laboratories. The carton contains one single-dose vial and displays the NDC code 68001-649-37.*
FDA Label Image

Carton (Leucovorin Calcium for Injection USP 350mg per vial)

Carton (Leucovorin Calcium for Injection USP 350mg per vial)
Packaging label for Leucovorin Calcium 350 mg per vial injection, lyophilized powder for intravenous or intramuscular use. The label indicates it is a single-dose vial manufactured for BluePoint Laboratories, with NDC 68001-650-38. Additional storage and preparation instructions are printed, along with a barcode and manufacturer details.*
FDA Label Image

Structural Formula (Leuco Structure)

Structural Formula (Leuco Structure)
Chemical structure of leucovorin calcium showing its molecular formula C20H21CaN7O7. The diagram depicts the arrangement of atoms and bonds in the leucovorin calcium molecule.*
FDA Label Image

Vial Label (Leucovorin Calcium for Injection USP 100mg per vial)

Vial Label (Leucovorin Calcium for Injection USP 100mg per vial)
Label for Leucovorin Calcium for Injection, USP 100 mg per vial, lyophilized powder for intravenous or intramuscular use. The single-dose vial contains calcium leucovorin equivalent to 10 mg leucovorin and 80 mg sodium chloride. Manufactured by Kindos Pharmaceuticals Co., Ltd., distributed by BluePoint Laboratories. Includes storage and usage instructions with a barcode and NDC 68001-648-36.*
FDA Label Image

Vial Label (Leucovorin Calcium for Injection USP 200mg per vial)

Vial Label (Leucovorin Calcium for Injection USP 200mg per vial)
Leucovorin calcium for injection, USP, 200 mg per vial, lyophilized powder in a single-dose vial for intravenous or intramuscular use. The label includes NDC 68001-649-37 and states it is Rx only. It is manufactured by Kindos Pharmaceuticals Co., Ltd. for BluePoint Laboratories, with dissolution and storage instructions included on the label.*
FDA Label Image

Vial Label (Leucovorin Calcium for Injection USP 350mg per vial)

Vial Label (Leucovorin Calcium for Injection USP 350mg per vial)
Label for Leucovorin Calcium for Injection, USP 350 mg per vial, lyophilized single-dose vial. The product is intended for intravenous or intramuscular use. The label includes dosage strength, administration route, storage instructions, and manufacturer information, BluePoint Laboratories. The vial is for prescription use only with NDC 68001-650-38.*

* 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.