Rasagiline Tablet
Product Images NDC 84386-169

3 FDA label images from Aurobindo Pharma Limited · 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 Rasagiline (NDC 84386-169). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Aurobindo 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

Chemical Structure (Rasagiline Str)

Chemical Structure (Rasagiline Str)
Chemical structure of Rasagiline, showing its core molecular framework with the associated sulfonic acid group (CH3SO3H). The illustration depicts the molecular arrangement relevant to the active ingredient Rasagiline.*
FDA Label Image

Package Label-principal Display Panel (0.5 mg (30 Tablets Bottle))

Package Label-principal Display Panel (0.5 mg (30 Tablets Bottle))
Rasagiline Tablets 0.5 mg oral tablets label by Aurobindo Pharma Limited. The 30-tablet bottle label shows NDC 84386-169-30, storage instructions, dispensing info, and distribution by Aurobindo Pharma USA, Inc. A barcode and imprint image of the tablet are also visible.*
FDA Label Image

Package Label-principal Display Panel (1 mg (30 Tablets Bottle))

Package Label-principal Display Panel (1 mg (30 Tablets Bottle))
Rasagiline Tablets 1 mg oral tablets label by Aurobindo Pharma Limited, featuring 30 tablets per container. The label includes dosage strength, manufacturer and distributor information (Aurobindo Pharma USA, Inc.), storage instructions, and a note about child-resistant packaging. It also shows a depiction of the tablet and a barcode on the right.*

* 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.