NDCFind

Bupropion Hydrochloride 82804-0123-30

Package NDC

82804-0123-30

Product NDC: 82804-0123

Manufacturer
Proficient Rx Lp
Dosage Form
Tablet, Film Coated
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
January 17, 2006
Listing Expires
December 31, 2026
Application
ANDA076143
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Active Ingredients

IngredientStrength
Bupropion Hydrochloride100 mg/1

Drug Class

Aminoketone [EPC]Dopamine Uptake Inhibitors [MoA]Increased Dopamine Activity [PE]

Selected Package

82804-0123-30Selected

30 TABLET, FILM COATED in 1 BOTTLE (82804-123-30)