NDCFind

Bupropion Hydrochloride 71335-2652-01

Package NDC

71335-2652-01

Product NDC: 71335-2652

Manufacturer
Bryant Ranch Prepack
Dosage Form
Tablet, Film Coated
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
April 25, 2024
Listing Expires
December 31, 2026
Application
ANDA075491
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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

71335-2652-01Selected

60 TABLET, FILM COATED in 1 BOTTLE (71335-2652-1)

Other packages for this product(6)

30 TABLET, FILM COATED in 1 BOTTLE (71335-2652-2)

100 TABLET, FILM COATED in 1 BOTTLE (71335-2652-3)

90 TABLET, FILM COATED in 1 BOTTLE (71335-2652-4)

120 TABLET, FILM COATED in 1 BOTTLE (71335-2652-5)

15 TABLET, FILM COATED in 1 BOTTLE (71335-2652-6)

21 TABLET, FILM COATED in 1 BOTTLE (71335-2652-7)