Bupropion Hydrochloride 60760-0781-30

Package NDC

60760-0781-30

Manufacturer: St. Mary's Medical Park Pharmacy
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: January 17, 2006
Listing Expires: December 31, 2026
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

60760-0781-30Selected

30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (60760-781-30)