NDCFind

Bupropion Hydrochloride Xl 70518-4014

Generic: Bupropion Hydrochloride

Product NDC

70518-4014
Manufacturer
Remedyrepack Inc.
Dosage Form
Tablet, Extended Release
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
February 7, 2024
Listing Expires
December 31, 2026
Application
ANDA210015
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Active Ingredients

IngredientStrength
Bupropion Hydrochloride300 mg/1

Drug Class

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

Packaging Options(2)

90 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4014-0)

30 TABLET, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (70518-4014-1)