Baclofen Tablet
Product Images NDC 72189-565

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 72189-565). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Direct_rx, 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

72189-565-60 (72189 565 60)

72189-565-60 (72189 565 60)
Baclofen 20 mg oral tablets, packaged in a container labeled for 60 tablets. The label shows the product name Baclofen, strength 20 mg, and quantity 60 tablets. It lists the generic name as Lioresal with each tablet containing Baclofen USP 20 mg. The labeler is Direct_rx and packaging details include lot SAMPLE, packager Direct, and a discard date of 6/2025. The label includes NDC 72189-565-60 and mentions the sample is from Dawsonsville, GA.*
FDA Label Image

72189-565-82 (72189 565 82)

72189-565-82 (72189 565 82)
Baclofen 20 mg oral tablets packaging label from Direct_rx. The label indicates 180 tablets per container. It is generic for Lioresal, with each tablet containing 20 mg of Baclofen (USP). The label includes NDC 72189-565-82 and distribution details for Direct_rx in Dawsonville, GA.*
FDA Label Image

72189-565-90 (72189 565 90)

72189-565-90 (72189 565 90)
Baclofen 20 mg tablet blister label by Direct_rx featuring a yellow background with black text. The label includes product name, strength (20 mg), and quantity (90 tablets). It states that each tablet contains Baclofen USP 20 mg as the active ingredient and is generic for Lioresal. Additional lot numbers, discard dates, and packaging information are listed on the sides.*

* 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.