Bupropion Hydrochloride Xl 00904-7469

Generic: Bupropion Hydrochloride

Product NDC

00904-7469

Manufacturer: Major Pharmaceuticals
Dosage Form: Tablet, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: October 7, 2024
Listing Expires: December 31, 2026
Application: ANDA090693

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Active Ingredients

Ingredient	Strength
Bupropion Hydrochloride	300 mg/1

Drug Class

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

Packaging Options(1)

00904-7469-04

30 BLISTER PACK in 1 CARTON (0904-7469-04) / 1 TABLET, EXTENDED RELEASE in 1 BLISTER PACK

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