NDCFind

Bupropion 65841-0836-10

Package NDC

65841-0836-10

Product NDC: 65841-0836

Manufacturer
Zydus Lifesciences Limited
Dosage Form
Tablet, Extended Release
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
August 2, 2018
Listing Expires
December 31, 2026
Application
ANDA201567
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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

65841-0836-10Selected

1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (65841-836-10)

Other packages for this product(3)

500 TABLET, EXTENDED RELEASE in 1 BOTTLE (65841-836-05)

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (65841-836-06)

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (65841-836-16)