Bafiertam Capsule
Product Images NDC 69387-001

3 FDA label images from Banner Life Sciences 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 Bafiertam (NDC 69387-001). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Banner Life Sciences 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

Bafiertam Structural Formula (Baf00 0002 01)

Bafiertam Structural Formula (Baf00 0002 01)
Chemical structure diagram of monomethyl fumarate, illustrating atoms and bonds including a carboxyl group and an ester group with a methyl substituent.*
FDA Label Image

Figure 1 (Baf00 0002 02)

Figure 1 (Baf00 0002 02)
A Kaplan-Meier curve showing the percentage of subjects with confirmed progression of disability over 96 weeks. The x-axis represents time on study in weeks, and the y-axis shows the percentage of subjects with confirmed progression. Two lines compare Placebo (n=408) and DMF 240 mg BID (n=409) groups, with the placebo group reaching approximately 27.1% and the DMF group 16.4% at 96 weeks. Confirmed progression criteria are noted in the figure.*
FDA Label Image

Principal Display Panel – Bottle Label (Baf00 0002 03)

Principal Display Panel – Bottle Label (Baf00 0002 03)
Label for BAFIERTAM delayed-release capsules containing 95 mg of monomethyl fumarate. The product is prescription-only, with 120 capsules per container. The label includes storage instructions, manufacturer details (Patheon Softgels Inc.), and labeler information (Banner Life Sciences LLC). The label features a barcode and the Banner Life Sciences logo.*

* 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.