Bupropion Hydrochloride 68071-3559-09

Package NDC

68071-3559-09

Manufacturer: Nucare Pharmaceuticals,inc.
Dosage Form: Tablet, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: June 14, 2017
Listing Expires: December 31, 2026
Application: ANDA090693

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Active Ingredients

Ingredient	Strength
Bupropion Hydrochloride	150 mg/1

Drug Class

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

Selected Package

68071-3559-09Selected

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68071-3559-9)