Bupropion Hydrochloride Xl 82009-0052-05

Generic: Bupropion Hydrochloride

Package NDC

82009-0052-05

Product NDC: 82009-0052

Manufacturer: Quallent Pharmaceuticals Health Llc
Dosage Form: Tablet, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: July 7, 2023
Listing Expires: December 31, 2027
Application: ANDA090693

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Active Ingredients

Ingredient	Strength
Bupropion Hydrochloride	300 mg/1

Drug Class

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

Selected Package

82009-0052-05Selected

500 TABLET, EXTENDED RELEASE in 1 BOTTLE (82009-052-05)