NDCFind

Bupropion Hydrochloride 63187-0713-60

Package NDC

63187-0713-60

Product NDC: 63187-0713

Manufacturer
Proficient Rx Lp
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
May 1, 2009
Listing Expires
December 31, 2026
Application
ANDA077415
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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

63187-0713-60Selected

60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-713-60)

Other packages for this product(2)

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-713-30)

90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (63187-713-90)