Bupropion Hydrochloride 59651-0874-01

Package NDC

59651-0874-01

Manufacturer: Aurobindo Pharma Limited
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: April 25, 2024
Listing Expires: December 31, 2026
Application: ANDA075491

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Active Ingredients

Ingredient	Strength
Bupropion Hydrochloride	75 mg/1

Drug Class

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

Selected Package

59651-0874-01Selected

100 TABLET, FILM COATED in 1 BOTTLE (59651-874-01)