NDCFind

Bupropion Hydrochloride 71335-0182-02

Package NDC

71335-0182-02

Product NDC: 71335-0182

Manufacturer
Bryant Ranch Prepack
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

71335-0182-02Selected

30 TABLET, FILM COATED in 1 BOTTLE (71335-0182-2)

Other packages for this product(6)

60 TABLET, FILM COATED in 1 BOTTLE (71335-0182-1)

100 TABLET, FILM COATED in 1 BOTTLE (71335-0182-3)

90 TABLET, FILM COATED in 1 BOTTLE (71335-0182-4)

120 TABLET, FILM COATED in 1 BOTTLE (71335-0182-5)

15 TABLET, FILM COATED in 1 BOTTLE (71335-0182-6)

21 TABLET, FILM COATED in 1 BOTTLE (71335-0182-7)