NDCFind

Bupropion Hydrochloride 47335-0954-81

Package NDC

47335-0954-81

Product NDC: 47335-0954

Manufacturer
Sun Pharmaceutical Industries, Inc.
Dosage Form
Tablet, Extended Release
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
December 25, 2014
Listing Expires
December 31, 2026
Application
ANDA200695
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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

47335-0954-81Selected

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-954-81)

Other packages for this product(2)

500 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-954-13)

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (47335-954-83)