NDCFind

Bupropion Hydrochloride 71335-0013-01

Package NDC

71335-0013-01

Product NDC: 71335-0013

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 Hydrochloride75 mg/1

Drug Class

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

Selected Package

71335-0013-01Selected

30 TABLET, FILM COATED in 1 BOTTLE (71335-0013-1)

Other packages for this product(6)

60 TABLET, FILM COATED in 1 BOTTLE (71335-0013-2)

90 TABLET, FILM COATED in 1 BOTTLE (71335-0013-3)

7 TABLET, FILM COATED in 1 BOTTLE (71335-0013-4)

14 TABLET, FILM COATED in 1 BOTTLE (71335-0013-5)

120 TABLET, FILM COATED in 1 BOTTLE (71335-0013-6)

100 TABLET, FILM COATED in 1 BOTTLE (71335-0013-7)