Pramipexole Dihydrochloride Tablet, Extended Release
Product Images NDC 33342-212

Product Visual Gallery

This gallery contains 15 technical images submitted to the FDA as part of the official labeling for Pramipexole Dihydrochloride (NDC 33342-212). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Macleods Pharmaceuticals 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

Pramipexole 0375mg 100s

Packaging label for Pramipexole Dihydrochloride Extended-Release Tablets 0.375 mg by Macleods Pharmaceuticals Limited. The label includes dosage strength prominently, batch and expiration details sections, and storage instructions. The package contains 100 tablets in a 10x10 unit dose format.*

FDA Label Image

Pramipexole 0375mg 30s

Label for Pramipexole Dihydrochloride Extended-Release Tablets 0.375 mg by Macleods Pharmaceuticals Limited. The label indicates once-daily oral tablets with 30 count per container. It includes dosage instructions to swallow tablets whole without chewing or dividing and storage conditions. Manufactured in India for Macleods Pharma USA, Inc.*

FDA Label Image

Pramipexole 075mg 100s

Pramipexole Dihydrochloride extended-release tablets 0.75 mg label from Macleods Pharmaceuticals Limited. The label indicates once-daily oral tablets in a package containing 100 unit dose tablets. It includes manufacturer and packaging details, batch number, expiration date, and a barcode.*

FDA Label Image

Pramipexole 075mg 30s

Label for Pramipexole Dihydrochloride Extended-Release Tablets 0.75 mg by Macleods Pharmaceuticals Limited. The label indicates 30 tablets in the container and specifies that tablets must be swallowed whole. It includes storage instructions and notes it is for prescription use only. Manufactured for Macleods Pharma USA, Inc.*

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Pramipexole 1 5mg 100s

Pramipexole Dihydrochloride Extended-Release Tablets 1.5 mg carton label from Macleods Pharmaceuticals Limited. The label indicates a 100-count package of unit dose tablets with barcode and manufacturing details. It specifies oral route and the tablet strength as 1.5 mg in extended-release form.*

FDA Label Image

Pramipexole 15mg 30s

Label for Pramipexole Dihydrochloride Extended-Release Tablets 1.5 mg by Macleods Pharmaceuticals Limited. The label indicates a once-daily oral tablet form with 30 tablets per container. It includes dosage instructions emphasizing tablets must be swallowed whole, storage information, and manufacturer details for Macleods Pharma USA, Inc. and Macleods Pharmaceuticals Ltd.*

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Pramipexole 225mg 100s

Packaging label for Pramipexole Dihydrochloride Extended-Release Tablets, 2.25 mg strength, for oral use. The label indicates a once-daily dosage and shows a 100-count (10 x 10) unit-dose carton of tablets. Manufactured by Macleods Pharmaceuticals Limited, the text includes lot and expiration date areas, a barcode, storage instructions, and a caution statement.*

FDA Label Image

Pramipexole 225mg 30s

Pramipexole Dihydrochloride Extended-Release Tablets 2.25 mg tablet label by Macleods Pharmaceuticals Limited. The label includes dosage strength, usage instructions noting tablets must be swallowed whole, storage conditions, and manufacturer information for Macleods Pharma USA, Inc. The package contains 30 tablets in the original unit dose container for oral use.*

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Pramipexole 3 75mg 100s

Packaging label for Pramipexole Dihydrochloride Extended-Release Tablets, 3.75 mg strength. The label indicates the product is for once daily oral use, containing 100 tablets in a unit-dose format. The labeler is Macleods Pharmaceuticals Limited, with manufacturing information for Macleods Pharma USA, Inc. The label includes a barcode, batch number, expiration date fields, and dosage instructions noting the tablets must be swallowed whole and not divided or crushed.*

FDA Label Image

Pramipexole 375mg 30s

Label for Pramipexole Dihydrochloride Extended-Release Tablets, 3.75 mg strength, oral dosage form. The label indicates this product is for once daily use and contains 30 tablets per container. It is manufactured by Macleods Pharmaceuticals Limited and Macleods Pharma USA, Inc. Storage and handling instructions are provided along with a barcode on the label.*

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Pramipexole 3mg 100s

Packaging label of Pramipexole Dihydrochloride Extended-Release Tablets 3 mg, manufactured by Macleods Pharmaceuticals Limited. The label indicates the product is for oral use, once daily dosing, with 100 tablets per bottle. The label includes batch and expiry date barcode and standard manufacturing information.*

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Pramipexole 3mg 30s

Label for Pramipexole Dihydrochloride Extended-Release Tablets, 3 mg strength, orally administered. The label indicates a 30-tablet count in the original unit of use container. Manufactured for Macleods Pharma USA, Inc. and Macleods Pharmaceuticals Ltd. Dosage instructions emphasize swallowing whole without chewing, crushing, or dividing. Storage and handling information is provided, including protection from high humidity and temperature guidelines.*

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Pramipexole 4 5mg 100s

Packaging label for Pramipexole Dihydrochloride Extended-Release Tablets 4.5 mg, once daily. The label shows 100 tablets in 10-unit dose packs. Manufactured and distributed by Macleods Pharmaceuticals Limited. The label includes product name, strength, dosage form, and information such as batch number and expiration date area, with a barcode visible.*

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Pramipexole 45mg 30s

Label for Pramipexole Dihydrochloride Extended-Release Tablets, 4.5 mg, oral dosage form by Macleods Pharmaceuticals Limited. The label specifies 30 tablets per container, for once daily use, with storage instructions and warnings. It includes both the manufacturer in the USA and India and dosage caution to swallow whole without chewing, crushing, or dividing.*

FDA Label Image

Prami (Pramipexole Structural Formula)

Chemical structure of Pramipexole Dihydrochloride, showing the molecular arrangement including a thiazole ring, amine groups, and dihydrochloride and hydrate components.*

* 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.