Bupropion Hydrochloride 70518-4674

Product NDC

70518-4674

Manufacturer: Remedyrepack Inc.
Dosage Form: Tablet, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: June 2, 2026
Listing Expires: December 31, 2027
Application: ANDA211020

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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)

70518-4674-00

30 TABLET, EXTENDED RELEASE in 1 BLISTER PACK (70518-4674-0)

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