Bupropion Hydrochloride Tablet, Film Coated, Extended Release
Product Images NDC 43598-536

Product Visual Gallery

This gallery contains 8 technical images submitted to the FDA as part of the official labeling for Bupropion Hydrochloride (NDC 43598-536). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Dr. Reddy�s Laboratories 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

Bupropion-hydrochloride-sr-1 (Bupropion Hydrochloride Sr 1)

Chemical structure of bupropion hydrochloride, showing the molecular arrangement including a chlorophenyl group and tert-butyl group linked to a ketone and hydrochloride salt.*

FDA Label Image

Bupropion-label1 (Bupropion Label1)

Label for Bupropion Hydrochloride SR Extended-Release Tablets USP (SR) 100 mg by Dr. Reddy's Laboratories Inc. The label indicates the medication is for twice-a-day use after initial titration and contains 60 film-coated extended-release tablets. It includes a warning against use with ZYBAN or medicines containing bupropion hydrochloride and advises pharmacists to dispense the Medication Guide with each prescription. The label also shows the NDC number and storage instructions.*

FDA Label Image

Bupropion-label2 (Bupropion Label2)

Label for Bupropion Hydrochloride SR Extended-Release Tablets USP (SR) 100 mg oral tablets. The label indicates a twice-a-day dosing after initial titration and includes a warning against use with ZYBAN or other bupropion hydrochloride-containing medicines. It specifies dispensing 100 tablets by Dr. Reddy's Laboratories Inc. The label also provides storage instructions and regulatory information, including NDC number 43598-536-01.*

FDA Label Image

Bupropion-label3 (Bupropion Label3)

Packaging label for Bupropion Hydrochloride SR, USP Extended-Release Tablets, 100 mg strength. The label shows the proprietary name as 'buPROPion HCl Extended-Release Tablets, USP (SR)' and includes a warning not to use the product in combination with Zyban or other medications containing bupropion hydrochloride. The tablet count is 500, and the product is labeled for oral use. Dr. Reddy's Laboratories Inc. is the manufacturer. The label also features the NDC 43598-536-05 and storage instructions.*

FDA Label Image

Bupropion-label4 (Bupropion Label4)

Bupropion Hydrochloride SR 150 mg extended-release film-coated tablets label from Dr. Reddy's Laboratories Inc. The label indicates a 60-tablet bottle with dosing instructions for twice-a-day use, a warning against use with ZYBAN or other products containing bupropion hydrochloride, and includes the NDC barcode and manufacturing details.*

FDA Label Image

Bupropion-label5 (Bupropion Label5)

The packaging label for Bupropion Hydrochloride SR Extended-Release Tablets, USP (SR), 150 mg strength. The label identifies the product as a twice-a-day dose after initial titration, with a total of 100 film-coated, extended-release oral tablets. It includes a pharmacist warning not to use the drug in combination with ZYBAN or other medicines containing bupropion hydrochloride. The label shows the NDC number 43598-537-01 and the manufacturer Dr. Reddy's Laboratories Inc.*

FDA Label Image

Bupropion-label6 (Bupropion Label6)

Label for Bupropion Hydrochloride Extended-Release Tablets USP (SR) 150 mg by Dr. Reddy's Laboratories Inc. The packaging is marked for 500 tablets and includes warnings about not using in combination with ZYBAN or other bupropion hydrochloride medicines. It features storage instructions, dosing advice, and a barcode.*

FDA Label Image

Bupropion-label7 (Bupropion Label7)

Label for Bupropion Hydrochloride SR Extended-Release Tablets 200 mg by Dr. Reddy's Laboratories Inc. The label indicates a package of 60 film-coated, extended-release tablets, with a warning against use with ZYBAN or other medicines containing bupropion hydrochloride. It includes NDC 43598-538-60 and storage instructions.*

* 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.