NDCFind

Bupropion Hydrochloride 70010-0784-09

Package NDC

70010-0784-09

Product NDC: 70010-0784

Manufacturer
Granules Pharmaceuticals Inc.
Dosage Form
Tablet, Extended Release
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
December 15, 2022
Listing Expires
December 31, 2027
Application
ANDA215568
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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

70010-0784-09Selected

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-784-09)

Other packages for this product(2)

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-784-03)

500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70010-784-05)