Bupropion Hydrochloride Sr 72189-0349-60

Package NDC

72189-0349-60

Manufacturer: Directrx
Dosage Form: Tablet, Film Coated, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: April 22, 2022
Listing Expires: December 31, 2026
Application: ANDA205794

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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

72189-0349-60Selected

60 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-349-60)

Other packages for this product(1)

72189-0349-30

30 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE (72189-349-30)

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