Methotrexate Tablet
Product Images NDC 48433-065

View Photos of 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 Methotrexate (NDC 48433-065). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Safecor Health 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

Methotrexate Structural Formula (Image 01)

Methotrexate Structural Formula (Image 01)
Chemical structure diagram of methotrexate, showing its molecular components, including aromatic rings and amino groups, consistent with its chemical composition as an active pharmaceutical ingredient.*
FDA Label Image

Methotrexate 2.5 mg Tablets, Usp Unit Carton Label (Image 02)

Methotrexate 2.5 mg Tablets, Usp Unit Carton Label (Image 02)
Methotrexate 2.5 mg oral tablets packaging label from Safecor Health LLC. The label includes the proprietary name Methotrexate, dosage form as tablets USP, strength 2.5 mg, and indicates the product is a cytotoxic agent. The package contains 20 tablets (2 x 10) and bears the NDC 48433-065-05. Manufacturer identified as Mylan Pharmaceuticals Inc. The label also includes storage instructions and a barcode.*
FDA Label Image

Unit Carton (Image 03)

Unit Carton (Image 03)
Packaging label for Methotrexate 2.5 mg oral tablets by Safecor Health LLC. The label features the UDL logo and designates the product as a unit dose package intended for institutional use only. It notes the container is not child resistant and provides light resistance to protect the contents. Distribution is by Safecor Health LLC, Rockford, IL.*

* 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.