NDCFind

Bupropion Hydrochloride 16571-0863-03

Package NDC

16571-0863-03

Product NDC: 16571-0863

Manufacturer
Rising Pharma Holdings, Inc.
Dosage Form
Tablet, Extended Release
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
August 1, 2022
Listing Expires
December 31, 2027
Application
ANDA211020
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Active Ingredients

IngredientStrength
Bupropion Hydrochloride300 mg/1

Drug Class

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

Selected Package

16571-0863-03Selected

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (16571-863-03)

Other packages for this product(3)

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (16571-863-09)

1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (16571-863-10)

500 TABLET, EXTENDED RELEASE in 1 BOTTLE (16571-863-50)