Pramipexole Dihydrochloride Tablet
Product Images NDC 65862-606

7 FDA label images from Aurobindo Pharma Limited · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 7 technical images submitted to the FDA as part of the official labeling for Pramipexole Dihydrochloride (NDC 65862-606). 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

Package Label-principal Display Panel (0.125 mg (90 Tablet Bottle))

Package Label-principal Display Panel (0.125 mg (90 Tablet Bottle))
Label for Pramipexole Dihydrochloride Tablets 0.125 mg by Aurobindo Pharma Limited. The label indicates the product contains 90 tablets with 0.125 mg strength, including dosage form and storage instructions. Distribution information for Aurobindo Pharma USA, Inc. is also shown, along with NDC and barcode details.*
FDA Label Image

Package Label-principal Display Panel (0.25 mg (90 Tablet Bottle))

Package Label-principal Display Panel (0.25 mg (90 Tablet Bottle))
Label for Pramipexole Dihydrochloride Tablets, 0.25 mg strength, packaged in a bottle of 90 tablets. The label shows the NDC 65862-605-90, indicates Rx only status, and displays storage instructions and dosage advisories. Manufactured by Aurobindo Pharma Limited, distributed by Aurobindo Pharma USA, Inc., and made in India.*
FDA Label Image

Package Label-principal Display Panel (0.5 mg (90 Tablet Bottle))

Package Label-principal Display Panel (0.5 mg (90 Tablet Bottle))
Label for Pramipexole Dihydrochloride Tablets 0.5 mg, a prescription drug distributed by Aurobindo Pharma USA, Inc. The label indicates a tablet dosage form with 90 tablets per container. It includes storage instructions, active ingredient content, and a barcode. The product is made in India by Aurobindo Pharma Limited.*
FDA Label Image

Package Label-principal Display Panel (0.75 mg (90 Tablet Bottle))

Package Label-principal Display Panel (0.75 mg (90 Tablet Bottle))
Label for Pramipexole Dihydrochloride Tablets 0.75 mg, a prescription drug distributed by Aurobindo Pharma USA, Inc. The label indicates each tablet contains 0.75 mg pramipexole dihydrochloride monohydrate and provides storage instructions (20° to 25°C) with a 90 tablet count. The product is made in India with a barcode on the right side.*
FDA Label Image

Package Label-principal Display Panel (1 mg (90 Tablet Bottle))

Package Label-principal Display Panel (1 mg (90 Tablet Bottle))
Label for Pramipexole Dihydrochloride Tablets, 1 mg strength. The label includes NDC 65862-608-90 and indicates the product is prescription only. It states each tablet contains 1 mg pramipexole dihydrochloride monohydrate equivalent to 0.94 mg pramipexole dihydrochloride USP. Distributed by Aurobindo Pharma USA, Inc. and made in India. The label also notes storage instructions and package count of 90 tablets.*
FDA Label Image

Package Label-principal Display Panel (1.5 mg (90 Tablets Bottle))

Package Label-principal Display Panel (1.5 mg (90 Tablets Bottle))
Label for Pramipexole Dihydrochloride Tablets 1.5 mg by Aurobindo Pharma Limited. The label states each tablet contains 1.5 mg pramipexole dihydrochloride monohydrate equivalent, with a count of 90 tablets. It includes storage instructions and distributor information for Aurobindo Pharma USA, Inc., featuring a barcode on the right side.*
FDA Label Image

Chemical Structure (Pramipexole Str)

Chemical Structure (Pramipexole Str)
Chemical structure of Pramipexole Dihydrochloride, depicted with indole and thiazole rings and associated chemical groups including dihydrochloride and water of hydration.*

* 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.