Bupropion Hydrochloride Sr 00904-7465

Generic: Bupropion Hydrochloride

Product NDC

00904-7465

Manufacturer: Major Pharmaceuticals
Dosage Form: Tablet, Film Coated, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: November 15, 2024
Listing Expires: December 31, 2027
Application: ANDA202304

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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]

Packaging Options(1)

00904-7465-61

100 BLISTER PACK in 1 CARTON (0904-7465-61) / 1 TABLET, FILM COATED, EXTENDED RELEASE in 1 BLISTER PACK

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