Baclofen
Product Images NDC 53808-1036

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 Baclofen (NDC 53808-1036). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by State Of Florida Doh Central Pharmacy, 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

Label Image For 10mg (10mg Qualitest)

Label Image For 10mg (10mg Qualitest)
Packaging label for Baclofen 10 mg tablets with a quantity of 30. The label indicates the product is Rx only and is labeled by State of Florida DOH Central Pharmacy, Tallahassee, FL 32304. The lot number and expiration date fields are present along with a barcode and UPC number.*
FDA Label Image

Label Image For 20mg (20mg Qualitest)

Label Image For 20mg (20mg Qualitest)
Packaging label for Baclofen 20 mg tablets distributed by State of Florida DOH Central Pharmacy. The label indicates a quantity of 30 tablets with a lot number C0490112A and an expiration date of September 30, 2013. Additional details include the packaging label being marked as RX only and the pharmacy location in Tallahassee, FL 32304, with a barcode and UPC number 306032407283.*
FDA Label Image

This Is An Image Of The Structural Formula For Baclofen. (Baclofentabs10mg20mg 1)

This Is An Image Of The Structural Formula For Baclofen. (Baclofentabs10mg20mg 1)
Chemical structure of Baclofen showing a chlorophenyl group attached to an amino acid backbone. The structure includes molecular formula C10H12ClNO2 and molecular weight 213.66.*

* 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.