Bupropion Hydrochloride 68084-0697-01

Package NDC

68084-0697-01

Manufacturer: American Health Packaging
Dosage Form: Tablet, Film Coated, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: April 2, 2015
Listing Expires: December 31, 2026
Application: ANDA079095

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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

68084-0697-01Selected

100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-697-01) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK (68084-697-11)