NDCFind

Bupropion Hydrochloride 69097-0072

Product NDC

69097-0072
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

IngredientStrength
Bupropion Hydrochloride300 mg/1

Drug Class

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

Packaging Options(1)

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