Bupropion Hydrochloride 00115-5445-13

Package NDC

00115-5445-13

Manufacturer: Amneal Pharmaceuticals Of New York Llc
Dosage Form: Tablet, Film Coated, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: December 3, 2004
Listing Expires: December 31, 2026
Application: ANDA076711

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Active Ingredients

Ingredient	Strength
Bupropion Hydrochloride	200 mg/1

Drug Class

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

Selected Package

00115-5445-13Selected

60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (0115-5445-13)