Pramipexole Dihydrochloride Tablet
Product Images NDC 64380-747

Product Visual Gallery

This gallery contains 10 technical images submitted to the FDA as part of the official labeling for Pramipexole Dihydrochloride (NDC 64380-747). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Strides Pharma Science 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

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Chemical structure of pramipexole dihydrochloride, showing its molecular framework with amine, sulfur, nitrogen atoms, and hydrochloride hydrate groups as part of its chemical composition.*

FDA Label Image

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Label for pramipexole dihydrochloride 0.125 mg tablets, an oral prescription drug by Strides Pharma Science Limited. The label states storage instructions, patient dispensing notes, and packaging contains 90 tablets. The label includes barcode, manufacturer and distributor details, and a designated space for batch details and expiration information.*

FDA Label Image

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Label for pramipexole dihydrochloride tablets, 0.25 mg strength, oral dosage form. The label indicates the product is manufactured by Strides Pharma Science Ltd. and distributed by Strides Pharma Inc. It contains 90 tablets and carries storage instructions and safety precautions. The NDC displayed is 64380-747-05.*

FDA Label Image

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Pramipexole dihydrochloride 0.25 mg tablets packaging label by Strides Pharma Science Limited. The carton states the product contains 100 unit dose tablets (10x10) for oral administration. It includes the NDC 64380-747-01 and notes that the product is Rx only. Storage instructions and manufacturer details are also visible.*

FDA Label Image

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Label for pramipexole dihydrochloride tablets 0.5 mg, oral dosage form, manufactured by Strides Pharma Science Limited and distributed by Strides Pharma Inc. The label indicates packaging of 90 tablets, with storage instructions, dispensing requirements, and regulatory details including NDC 64380-748-05.*

FDA Label Image

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Packaging label for pramipexole dihydrochloride tablets 0.5 mg from Strides Pharma Science Limited. The label indicates 100 (10x10) unit dose tablets with instructions for storage and pediatric safety. It includes manufacturer and distributor information along with the NDC code 64380-748-01.*

FDA Label Image

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Label for pramipexole dihydrochloride tablets, 0.75 mg strength, in a package containing 90 tablets. Manufactured by Strides Pharma Science Ltd., Bengaluru, India, and distributed by Strides Pharma Inc., East Brunswick, NJ. The label includes storage instructions, dosage advisory, and barcode information.*

FDA Label Image

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Label for Pramipexole Dihydrochloride Tablets 1 mg in a 90-tablet supply. The label includes storage instructions, manufacturer and distributor information (Strides Pharma Science Ltd. and Strides Pharma Inc.), a barcode, and a space for batch details. It notes dispensing with patient information leaflet and Rx-only status.*

FDA Label Image

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Pramipexole dihydrochloride 1 mg oral tablets packaging label from Strides Pharma Inc. The label indicates 100 unit dose tablets in a 10x10 count configuration. It includes storage instructions, pharmacist dispensing information, and manufacturer details from Strides Pharma Science Ltd, India. The label is primarily white and pink with barcodes and NDC 64380-750-01.*

FDA Label Image

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Label for Pramipexole Dihydrochloride Tablets 1.5 mg, oral dosage form in a package of 90 tablets. The label includes storage instructions, a warning to protect from light, and distribution by Strides Pharma Inc. Manufactured by Strides Pharma Science Ltd. The label features the NDC 64380-751-05 and notes the prescription-only status.*

* 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.