NDCFind

Bupropion Hydrochloride Sr 50228-0176-60

Generic: Bupropion Hydrochloride

Package NDC

50228-0176-60

Product NDC: 50228-0176

Manufacturer
Sciegen Pharmaceuticals, Inc.
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
April 20, 2018
Listing Expires
December 31, 2027
Application
ANDA205794
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Active Ingredients

IngredientStrength
Bupropion Hydrochloride200 mg/1

Drug Class

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

Selected Package

50228-0176-60Selected

60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-176-60)

Other packages for this product(3)

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-176-01)

1000 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-176-10)

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (50228-176-30)