Bupropion Hydrochloride 69097-0072-12

Package NDC

69097-0072-12

Manufacturer: Cipla Usa., Inc.
Dosage Form: Tablet, Film Coated, Extended Release
Route: Oral
Product Type: Human Prescription Drug
Marketing Start: October 25, 2023
Listing Expires: December 31, 2026
Application: ANDA207479

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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]

Selected Package

69097-0072-12Selected

500 TABLET, FILM COATED, EXTENDED RELEASE in 1 BOTTLE, PLASTIC (69097-072-12)