NDCFind

Bupropion Hydrochloride 72189-0134-72

Package NDC

72189-0134-72

Product NDC: 72189-0134

Manufacturer
Direct Rx
Dosage Form
Tablet, Extended Release
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
October 15, 2020
Listing Expires
December 31, 2026
Application
ANDA210497
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Active Ingredients

IngredientStrength
Bupropion Hydrochloride150 mg/1

Drug Class

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

Selected Package

72189-0134-72Selected

120 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-134-72)

Other packages for this product(3)

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-134-30)

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-134-60)

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (72189-134-90)