NDCFind

Bupropion Hydrochloride 63304-0724-05

Package NDC

63304-0724-05

Product NDC: 63304-0724

Manufacturer
Sun Pharmaceutical Industries, Inc.
Dosage Form
Tablet, Extended Release
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
January 1, 2021
Listing Expires
December 31, 2026
Application
ANDA203650
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Active Ingredients

IngredientStrength
Bupropion Hydrochloride300 mg/1

Drug Class

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

Selected Package

63304-0724-05Selected

500 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-724-05)

Other packages for this product(2)

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-724-30)

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (63304-724-90)