Bupropion Hydrochloride 00904-6636-61

Package NDC

00904-6636-61

Manufacturer: Major Pharmaceuticals
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: January 17, 2006
Listing Expires: December 31, 2027
Application: ANDA076143

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Active Ingredients

Ingredient	Strength
Bupropion Hydrochloride	100 mg/1

Drug Class

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

Selected Package

00904-6636-61Selected

100 BLISTER PACK in 1 CARTON (0904-6636-61) / 1 TABLET, FILM COATED in 1 BLISTER PACK