NDCFind

Bupropion 68382-0353-05

Package NDC

68382-0353-05

Product NDC: 68382-0353

Manufacturer
Zydus Pharmaceuticals Usa Inc.
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

68382-0353-05Selected

500 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-353-05)

Other packages for this product(3)

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-353-06)

1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-353-10)

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68382-353-16)