NDCFind

Bupropion 51655-0357-52

Generic: Bupropion Hydrochloride

Package NDC

51655-0357-52

Product NDC: 51655-0357

Manufacturer
Northwind Health Company, Llc
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
May 28, 2020
Listing Expires
December 31, 2027
Application
ANDA202304
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Active Ingredients

IngredientStrength
Bupropion Hydrochloride150 mg/1

Drug Class

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

Selected Package

51655-0357-52Selected

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-357-52)

Other packages for this product(1)

90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (51655-357-26)