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Bupropion Hydrochloride - 66336-897-30 - (Bupropion Hydrochloride)

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Drug Information of Bupropion Hydrochloride

Product NDC: 66336-897
Proprietary Name: Bupropion Hydrochloride
Non Proprietary Name: Bupropion Hydrochloride
Active Ingredient(s): 150    mg/1 & nbsp;   Bupropion Hydrochloride
Administration Route(s): OCCLUSIVE DRESSING TECHNIQUE
Dosage Form(s): TABLET
Coding System: National Drug Codes(NDC)

Labeler Information of Bupropion Hydrochloride

Product NDC: 66336-897
Labeler Name: Dispensing Solutions, Inc.
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number: ANDA077455
Marketing Category: ANDA
Start Marketing Date: 20080312

Package Information of Bupropion Hydrochloride

Package NDC: 66336-897-30
Package Description: 30 TABLET in 1 BOTTLE (66336-897-30)

NDC Information of Bupropion Hydrochloride

NDC Code 66336-897-30
Proprietary Name Bupropion Hydrochloride
Package Description 30 TABLET in 1 BOTTLE (66336-897-30)
Product NDC 66336-897
Product Type Name HUMAN PRESCRIPTION DRUG
Non Proprietary Name Bupropion Hydrochloride
Dosage Form Name TABLET
Route Name OCCLUSIVE DRESSING TECHNIQUE
Start Marketing Date 20080312
Marketing Category Name ANDA
Labeler Name Dispensing Solutions, Inc.
Substance Name BUPROPION HYDROCHLORIDE
Strength Number 150
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 Bupropion Hydrochloride


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