Bupropion Hydrochloride Tablet, Film Coated, Extended Release
Product Images NDC 50228-174

15 FDA label images from Sciegen Pharmaceuticals, Inc. · Packaging, Regulatory Labels, and Product Appearance

Product Visual Gallery

This gallery contains 15 technical images submitted to the FDA as part of the official labeling for Bupropion Hydrochloride (NDC 50228-174). Unlike standard consumer photos, these assets often include clinical data figures, molecular chemical structures, and official manufacturer packaging layouts.

As provided by Sciegen 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

Bupropion HCl 100 mg 1,000 Extended-release Tablet, Usp Label (Bupropion 100mg 1000tab)

Bupropion HCl 100 mg 1,000 Extended-release Tablet, Usp Label (Bupropion 100mg 1000tab)
Label for buPROPion HCl Extended-Release Tablets, USP (SR), 100 mg strength, film-coated extended-release oral tablets by ScieGen Pharmaceuticals, Inc. The label states a 1,000 tablet count with instructions for pharmacist dispensing and warnings about interactions with other bupropion-containing medicines. It includes storage information, lot, expiration date, and barcode.*
FDA Label Image

Bupropion HCl 100 mg 100 Extended-release Tablet, Usp Label (Bupropion 100mg 100tab)

Bupropion HCl 100 mg 100 Extended-release Tablet, Usp Label (Bupropion 100mg 100tab)
Label for Bupropion Hydrochloride SR extended-release tablets, USP, 100 mg strength. The label indicates the tablet is for oral use, comes in a 100-count bottle, and is labeled Twice-A-Day (After Initial Titration). It is manufactured by ScieGen Pharmaceuticals, Inc., Hauppauge, NY. The label includes storage instructions, warnings, dosage information, and a barcode.*
FDA Label Image

Bupropion HCl 100 mg 30 Extended-release Tablet, Usp Label (Bupropion 100mg 30tab)

Bupropion HCl 100 mg 30 Extended-release Tablet, Usp Label (Bupropion 100mg 30tab)
Label for buPROPion HCl Extended-Release Tablets, USP (SR) 100 mg by ScieGen Pharmaceuticals, Inc. The label states it is a twice-a-day (after initial titration) oral tablet, extended-release formulation. It includes prescription-only status, a warning against use with Zyban or other bupropion hydrochloride medicines, a quantity of 30 tablets, storage directions, and manufacturer details from Hauppauge, NY.*
FDA Label Image

Bupropion HCl 100 mg 500 Extended-release Tablet, Usp Label (Bupropion 100mg 500tab)

Bupropion HCl 100 mg 500 Extended-release Tablet, Usp Label (Bupropion 100mg 500tab)
Label for Bupropion Hydrochloride SR 100 mg extended-release oral tablets, USP, manufactured by ScieGen Pharmaceuticals, Inc. The label indicates 500 film-coated extended-release tablets per container with instructions to dispense with the accompanying medication guide. Storage instructions specify 20° to 25°C, and warnings advise against use with ZYBAN or similar products containing bupropion hydrochloride.*
FDA Label Image

Bupropion HCl 100 mg 60 Extended-release Tablet, Usp Labell (Bupropion 100mg 60tab)

Bupropion HCl 100 mg 60 Extended-release Tablet, Usp Labell (Bupropion 100mg 60tab)
Label for Bupropion Hydrochloride SR 100 mg extended-release oral tablets by ScieGen Pharmaceuticals, Inc. The label indicates 60 tablets per container with use instructions to dispense a medication guide. It includes storage instructions, warnings, and manufacturer information, along with a barcode and NDC 50228-174-60.*
FDA Label Image

Bupropion HCl 150 mg 1,000 Extended-release Tablet, Usp Label (Bupropion 150mg 1000tab)

Bupropion HCl 150 mg 1,000 Extended-release Tablet, Usp Label (Bupropion 150mg 1000tab)
Label for Bupropion Hydrochloride SR 150 mg extended-release oral tablets from ScieGen Pharmaceuticals, Inc. The label shows the NDC 50228-175-10 for a 1,000 tablet package intended for twice-a-day dosing after initial titration. It includes usage warnings and pharmacist instructions, along with storage information and barcodes. The label indicates Rx only status and notes the product contains no varnish area on the tablet.*
FDA Label Image

Bupropion HCl 150 mg 100 Extended-release Tablet, Usp Label (Bupropion 150mg 100tab)

Bupropion HCl 150 mg 100 Extended-release Tablet, Usp Label (Bupropion 150mg 100tab)
Label for Bupropion Hydrochloride SR Extended-Release Tablets, USP (SR) 150 mg by ScieGen Pharmaceuticals, Inc. The label specifies a 100-count bottle of oral film-coated extended-release tablets with dosage instructions, storage conditions, and warnings. The label includes the NDC 50228-175-01 and states the product is Rx only.*
FDA Label Image

Bupropion HCl 150 mg 30 Extended-release Tablet, Usp Label (Bupropion 150mg 30tab)

Bupropion HCl 150 mg 30 Extended-release Tablet, Usp Label (Bupropion 150mg 30tab)
Label for Bupropion Hydrochloride SR Extended-Release Tablets, USP (SR) 150 mg by ScieGen Pharmaceuticals, Inc. The label indicates a 30 tablet bottle with dosage instructions for oral use twice-a-day after initial titration. It includes warnings about not combining with ZYBAN® or other bupropion-containing medicines and displays the NDC number 50228-175-30.*
FDA Label Image

Bupropion HCl 150 mg 500 Extended-release Tablet, Usp Label (Bupropion 150mg 500tab)

Bupropion HCl 150 mg 500 Extended-release Tablet, Usp Label (Bupropion 150mg 500tab)
Label for Bupropion Hydrochloride SR extended-release tablets, USP (SR) 150 mg by ScieGen Pharmaceuticals, Inc. The label states each tablet contains 150 mg bupropion hydrochloride and includes storage instructions, warnings, and dispensing information. The package size is 500 tablets, marked Rx only. A barcode and NDC number 50228-175-05 are also visible.*
FDA Label Image

Bupropion HCl 150 mg 60 Extended-release Tablet, Usp Label (Bupropion 150mg 60tab)

Bupropion HCl 150 mg 60 Extended-release Tablet, Usp Label (Bupropion 150mg 60tab)
Label for Bupropion HCl Extended-Release Tablets, USP (SR) 150 mg by ScieGen Pharmaceuticals, Inc. The label indicates 60 film-coated extended-release tablets with oral route, NDC 50228-175-60. It includes dosage, storage, and dispensing instructions with a barcode and a note that the product is Rx only.*
FDA Label Image

Bupropion HCl 200 mg 1,000 Extended-release Tablet, Usp Label (Bupropion 200mg 1000tab)

Bupropion HCl 200 mg 1,000 Extended-release Tablet, Usp Label (Bupropion 200mg 1000tab)
Label for Bupropion Hydrochloride SR 200 mg extended-release tablets by ScieGen Pharmaceuticals, Inc. The label highlights the product name, strength, and dosage form, with directions for pharmacist dispensing and warnings about medication combinations. It includes lot, expiration, barcode, and storage instructions for 1,000 tablets.*
FDA Label Image

Bupropion-200mg-100tab (Bupropion 200mg 100tab)

Bupropion-200mg-100tab (Bupropion 200mg 100tab)
Label for Bupropion Hydrochloride SR extended-release tablets USP, 200 mg strength, manufactured by ScieGen Pharmaceuticals, Inc. The label includes dosage form as film-coated extended-release tablets, prescription only, package count of 100 tablets, storage instructions, a warning about concomitant use with ZYBAN, and a UPC barcode. Tablet dimensions are noted as 0.90" x 1.5" with no varnish.*
FDA Label Image

Bupropion HCl 200 mg 30 Extended-release Tablet, Usp Label (Bupropion 200mg 30tab)

Bupropion HCl 200 mg 30 Extended-release Tablet, Usp Label (Bupropion 200mg 30tab)
Label for Bupropion HCl Extended-Release Tablets, USP (SR) 200 mg by ScieGen Pharmaceuticals, Inc. The label indicates a 30-tablet bottle with oral tablet dosage form. Dosing instructions specify twice-a-day use after initial titration. The label includes a warning against combining with ZYBAN or other bupropion hydrochloride medicines. Manufacturer information, storage instructions, lot, and expiration date fields are also present.*
FDA Label Image

Bupropion HCl 200 mg 60 Extended-release Tablet, Usp Label (Bupropion 200mg 60tab)

Bupropion HCl 200 mg 60 Extended-release Tablet, Usp Label (Bupropion 200mg 60tab)
Bupropion Hydrochloride SR 200 mg extended-release tablets film coated, packaged 60 tablets per bottle. The label includes dosage information, storage instructions, and warnings. The product is labeled for oral use and manufactured by ScieGen Pharmaceuticals, Inc. The label also states Rx Only and includes the NDC 50228-176-60 barcode.*
FDA Label Image

Chemical Structure (Bupropion Hydrochloride Sr 1)

Chemical Structure (Bupropion Hydrochloride Sr 1)
Chemical structure of bupropion hydrochloride, showing a chlorophenyl group and other functional groups characteristic of this compound.*

* 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.