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WELLBUTRIN XL - 21695-138-15 - (bupropion hydrochloride)

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Drug Information of WELLBUTRIN XL

Product NDC: 21695-138
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: 21695-138
Labeler Name: Rebel Distributors Corp
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: NDA021515
Marketing Category: NDA
Start Marketing Date: 20091223

Package Information of WELLBUTRIN XL

Package NDC: 21695-138-15
Package Description: 15 TABLET, EXTENDED RELEASE in 1 BOTTLE (21695-138-15)

NDC Information of WELLBUTRIN XL

NDC Code 21695-138-15
Proprietary Name WELLBUTRIN XL
Package Description 15 TABLET, EXTENDED RELEASE in 1 BOTTLE (21695-138-15)
Product NDC 21695-138
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name bupropion hydrochloride
Dosage Form Name TABLET, EXTENDED RELEASE
Route Name ORAL
Start Marketing Date 20091223
Marketing Category Name NDA
Labeler Name Rebel Distributors Corp
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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