NDCFind

Bupropion Hydrochloride Sr 71335-0135-05

Generic: Bupropion Hydrochloride

Package NDC

71335-0135-05

Product NDC: 71335-0135

Manufacturer
Bryant Ranch Prepack
Dosage Form
Tablet, Film Coated, Extended Release
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
July 2, 2009
Listing Expires
December 31, 2026
Application
ANDA079095
StockMeds — pharmacy-to-pharmacy marketplace

Need to source Bupropion Hydrochloride Sr? P2P pharmacy marketplace.

Find Supply →Sponsored

Active Ingredients

IngredientStrength
Bupropion Hydrochloride150 mg/1

Drug Class

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

Selected Package

71335-0135-05Selected

45 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-5)

Other packages for this product(8)

60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-1)

90 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-2)

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-3)

120 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-4)

180 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-6)

28 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-7)

56 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-8)

100 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (71335-0135-9)