Baclofen Tablet
Product Images NDC 72888-202

View Photos of Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Baclofen (NDC 72888-202). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Advagen Pharma Limited, 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

Ndc 72888-010-00 (Baclofen Tablets, USP 10 mg)

Ndc 72888-010-00 (Baclofen Tablets, USP 10 mg)
Label for Baclofen Tablets, USP 10 mg, oral tablets distributed by Advagen Pharma Limited and manufactured by Rubicon Research Private Limited. The label includes dosage strength, quantity of 1000 tablets, storage instructions, and manufacturer and distributor addresses. The label features a blue square with the product name and strength prominently displayed.*
FDA Label Image

Ndc 72888-010-01 (Baclofen Tablets, USP 10 mg)

Ndc 72888-010-01 (Baclofen Tablets, USP 10 mg)
Baclofen Tablets, USP 10 mg label for oral use, packaged in a container of 100 tablets. The label displays the NDC 72888-010-01 and states the active ingredient Baclofen, USP 10 mg per tablet. Distributed by Advagen Pharma Limited, Plainsboro, NJ, and manufactured by Rubicon Research Private Limited, India. Storage instructions specify 20° to 25°C. Includes warnings to keep medication out of children's reach and dispensing guidance.*
FDA Label Image

Ndc 72888-010-05 (Baclofen Tablets, USP 10 mg)

Ndc 72888-010-05 (Baclofen Tablets, USP 10 mg)
Label for Baclofen Tablets USP 10 mg, oral tablets distributed by Advagen Pharma Limited. The label states each tablet contains 10 mg baclofen and includes storage instructions, a child-resistant closure notice, and an NDC number (72888-010-05). It indicates a package size of 500 tablets and notes the manufacturer as Rubicon Research Private Limited in India.*
FDA Label Image

Ndc 72888-011-00 (Baclofen Tablets, USP 20 mg)

Ndc 72888-011-00 (Baclofen Tablets, USP 20 mg)
Label for Baclofen Tablets USP 20 mg by Advagen Pharma Limited. The label indicates the active ingredient Baclofen 20 mg per tablet, packaging contains 1000 tablets, and includes storage instructions and distributor/manufacturer details. The label features a prominent orange box with product name and strength in white text.*
FDA Label Image

Ndc 72888-011-01 (Baclofen Tablets, USP 20 mg)

Ndc 72888-011-01 (Baclofen Tablets, USP 20 mg)
Label for Baclofen Tablets, USP 20 mg oral tablets by Advagen Pharma Limited. The label states each tablet contains 20 mg of Baclofen, with a package size of 100 tablets. It includes storage instructions and manufacturer information for Rubicon Research Private Limited, India, barcode, and a caution to keep medication out of children's reach.*
FDA Label Image

Ndc 72888-011-05 (Baclofen Tablets, USP 20 mg)

Ndc 72888-011-05 (Baclofen Tablets, USP 20 mg)
Label for Baclofen Tablets, USP 20 mg, showing the quantity of 500 tablets. The label includes the distributor Advagen Pharma Limited in Plainsboro, NJ, and the manufacturer Rubicon Research Private Limited in India. It displays storage instructions, child safety warnings, and barcodes, with an orange block highlighting the product strength.*
FDA Label Image

Ndc 72888-009-01 (Baclofen Tablets, USP 5 mg)

Ndc 72888-009-01 (Baclofen Tablets, USP 5 mg)
Label for Baclofen Tablets, USP 5 mg by Advagen Pharma Limited, containing 100 oral tablets. The label includes dosage strength, storage instructions (20° to 25°C), child-resistant container requirement, and distributor and manufacturer details (Rubicon Research Private Limited, India). It features barcode and product NDC 72888-009-01.*
FDA Label Image

Baclofen Tab Usp Structure

Baclofen Tab Usp Structure
Chemical structure of baclofen showing a chlorophenyl group attached to a gamma-aminobutyric acid (GABA) backbone with molecular substitutions as depicted.*

* 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.