Dimethyl Fumarate Kit
Product Images NDC 31722-680

Product Visual Gallery

This gallery contains 11 technical images submitted to the FDA as part of the official labeling for Dimethyl Fumarate (NDC 31722-680). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Camber Pharmaceuticals, Inc., 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

1 (1)

Packaging label for Dimethyl Fumarate delayed-release capsules 30-day starter pack by Camber Pharmaceuticals, Inc. The label shows two doses: 120 mg starter dose (14 capsules in one bottle) and 240 mg regular dose (46 capsules in another bottle). It includes storage instructions, package contents, and manufacturer details, with dosing instructions and contact information.*

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2 (2)

Label for Dimethyl Fumarate Delayed-Release Capsules 120 mg by Camber Pharmaceuticals, Inc. The label indicates the product is prescription only with 14 capsules per container. It includes dosage instructions, storage requirements, a barcode, and manufacturer information. The label displays the NDC 31722-657-31 and highlights the 120 mg strength.*

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3 (3)

Packaging label for Dimethyl Fumarate delayed-release capsules, 120 mg strength, by Camber Pharmaceuticals, Inc. The carton includes dosage form and strength prominently, NDC 31722-657-31, with instructions to swallow whole and dispense in original package. It contains 14 capsules and notes storage conditions, usual dosage, and contact information for patient guidance. Manufactured for Camber Pharmaceuticals in Piscataway, NJ, with barcode and manufacturing license information visible.*

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Label for Dimethyl Fumarate delayed-release capsules, 240 mg strength, from Camber Pharmaceuticals, Inc. The label states the capsules should be swallowed whole, with a quantity of 60 capsules per bottle, and indicates Rx only. It includes storage instructions, contact information, and manufacturer details, along with a barcode and a note about an unvarnished area for batch coding.*

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Dimethyl Fumarate 240 mg delayed-release capsules packaging label from Camber Pharmaceuticals, Inc. The label shows the product strength, dosage form, and quantity of 60 capsules. It includes storage instructions, manufacturer information, a barcode, and a contact number for U.S. customers.*

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6 (6)

Dimethyl Fumarate 240 mg delayed-release capsules label by Camber Pharmaceuticals, Inc. The label indicates 46 capsules per container, with instructions to swallow capsules whole and that the product is prescription only. It includes storage instructions, dosage guidance, a barcode, and manufacturer details from Hetero Labs Limited, Hyderabad, India.*

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Dimethyl Fumarate delayed-release capsules 240 mg carton from Camber Pharmaceuticals, Inc. The label shows the proprietary name, strength, dosage form, NDC 31722-658-31, and states to swallow the capsule whole. It indicates 46 capsules per package and includes storage instructions, manufacturer details, and contact information.*

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Camber (Camber)

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Dimethylfumaratedrcapfigure1 (Dimethylfumaratedrcapfigure1)

A Kaplan-Meier curve chart showing the percentage of subjects with confirmed progression of disability over 96 weeks, comparing placebo (n=408) and dimethyl fumarate delayed-release capsules 240 mg (n=409). The y-axis represents the percentage of subjects, and the x-axis represents time on study in weeks. The chart illustrates higher progression in the placebo group (27.1%) versus the treatment group (16.4%).*

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Dimethylfumaratestructure (Dimethylfumaratestructure)

Chemical structure of dimethyl fumarate showing its molecular connectivity with characteristic ester functional groups and a double bond in the fumarate backbone.*

* 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.