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WELLBUTRIN XL - 54868-4935-0 - (bupropion hydrochloride)

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Drug Information of WELLBUTRIN XL

Product NDC: 54868-4935
Proprietary Name: WELLBUTRIN XL
Non Proprietary Name: bupropion hydrochloride
Active Ingredient(s): 300    mg/1 & nbsp;   bupropion hydrochloride
Administration Route(s): ORAL
Dosage Form(s): TABLET, EXTENDED RELEASE
Coding System: National Drug Codes(NDC)

Labeler Information of WELLBUTRIN XL

Product NDC: 54868-4935
Labeler Name: Physicians Total Care, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021515
Marketing Category: NDA
Start Marketing Date: 20031008

Package Information of WELLBUTRIN XL

Package NDC: 54868-4935-0
Package Description: 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-4935-0)

NDC Information of WELLBUTRIN XL

NDC Code 54868-4935-0
Proprietary Name WELLBUTRIN XL
Package Description 30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (54868-4935-0)
Product NDC 54868-4935
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name bupropion hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20031008
Marketing Category Name NDA
Labeler Name Physicians Total Care, Inc.
Substance Name BUPROPION HYDROCHLORIDE
Strength Number 300
Strength Unit mg/1
Pharmaceutical Classes Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA]

Complete Information of WELLBUTRIN XL


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