Dimethyl Fumarate
Product Images NDC 70771-1532

3 FDA label images from Zydus Lifesciences Limited · 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 Dimethyl Fumarate (NDC 70771-1532). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Zydus Lifesciences Limited, 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

Label (F97ea60b 3e1d 4040 9d97 D9df73851434 03)

Label (F97ea60b 3e1d 4040 9d97 D9df73851434 03)
Dimethyl fumarate delayed-release capsules 120 mg starter dose and 240 mg regular dose in a 30-day starter pack. Packaging shows one bottle with 14 capsules of 120 mg and one bottle with 46 capsules of 240 mg. Labeler is Zydus Lifesciences Limited. Directions for use and storage information are also included on the label.*
FDA Label Image

Label (F97ea60b 3e1d 4040 9d97 D9df73851434 04)

Label (F97ea60b 3e1d 4040 9d97 D9df73851434 04)
Label for Dimethyl Fumarate Delayed-Release Capsules 120 mg by Zydus Lifesciences Limited. The label shows a half green, half white capsule marked 1204, indicates 14 capsules per package, prescription only. Storage and dosage instructions with manufacturer Cadila Healthcare Ltd, India are included.*
FDA Label Image

Label (F97ea60b 3e1d 4040 9d97 D9df73851434 05)

Label (F97ea60b 3e1d 4040 9d97 D9df73851434 05)
Dimethyl Fumarate Delayed-Release Capsules 240 mg label showing a blue-green capsule with imprint '1205'. The label includes dosage strength, 46 capsules count, and manufacturer listed as Cadila Healthcare Ltd., Ahmedabad, India. It also features Zydus Pharmaceuticals logo and storage and dosage instructions.*

* 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.