Bupropion Hydrochloride 70518-4218

Product NDC

70518-4218

Manufacturer: Remedyrepack Inc.
Dosage Form: Tablet, Film Coated
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: October 21, 2024
Listing Expires: December 31, 2027
Application: ANDA203013

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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]

Packaging Options(2)

70518-4218-00

30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4218-0)

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70518-4218-01

90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-4218-1)

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