Bupropion Hydrochloride Tablet, Extended Release
Product Images NDC 68071-3928

Product Visual Gallery

This gallery contains 4 technical images submitted to the FDA as part of the official labeling for Bupropion Hydrochloride (NDC 68071-3928). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Nucare Pharmaceuticals,inc., 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

Pdp (68071 3928 9)

Label for Bupropion Hydrochloride XL 300 mg extended-release oral tablets, distributed by NuCare Pharmaceuticals, Inc. The package contains 90 tablets. The label includes product and lot information, storage instructions to keep at 58-77°F, and warnings to keep out of reach of children. Manufactured by Lupin Limited Goa, India.*

FDA Label Image

Image (8d9e24d7 369e 43b6 83be Babf9d9cf3e3 01)

Chemical structure of bupropion hydrochloride, showing the aromatic ring with chlorophenyl group, ketone group, amine group, and the hydrochloride moiety.*

FDA Label Image

Image (Dbdd8397 08cd 4e0a B545 601a288c195c 1475 1)

Bupropion Hydrochloride XL 300 mg extended-release oral tablets, labeled by NuCare Pharmaceuticals, Inc. The image shows a white container bottle with a white child-resistant cap. The bottle label includes the product name, strength, dosage form, and manufacturer information. A black floral graphic is visible near the bottom of the label.*

FDA Label Image

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Bupropion Hydrochloride XL 300 mg extended-release oral tablets by NuCare Pharmaceuticals, Inc. The image shows a blister pack containing 10 tablet compartments arranged with a line and circle pattern, consistent with a prescription drug packaging.*

* 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.