Baclofen Tablet
Product Images NDC 72189-504

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Baclofen (NDC 72189-504). 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

72189-0504-60 (72189 00504 60)

Baclofen 20 mg oral tablets packaging label showing 60 tablets per bottle. The label includes the product name Baclofen, strength 20 mg, and quantity of 60 tablets. The labeler is Direct_Rx. It states the generic name Baclofen with USP 20 mg per tablet and packaging information including lot and expiration dates.*

FDA Label Image

72189-504-90 (72189 504 90)

Packaging label for Baclofen 20 mg oral tablets by Direct_Rx. The label states each bottle contains 90 tablets of Baclofen, USP 20 mg. It includes the NDC number 72189-504-90 and notes this is a sample package with lot number SAMPLE and discard date 4/30/26. Distributor information is also visible.*

FDA Label Image

72189-504-82 (72189 504 82)

Box label for Baclofen 20 mg oral tablets by DirectRx, containing 180 tablets. The label indicates the product is generic for Lioresal and each tablet contains 20 mg of Baclofen, USP. The lot number is SAMPLE with an expiration date of 5/31/26, packaged and distributed by DirectRx in Dawsonville, GA.*

FDA Label Image

72189-504-30 (72189 504 30)

Label for Baclofen 20 mg oral tablets, containing 30 tablets per package. The product is generic for Lioresal and is distributed by Direct Rx. The label includes storage instructions, lot number, expiration date (6/30/27), and packaging location in Dawsonville, GA.*

* 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.