NDCFind

Bupropion Hydrochloride 71335-1214-05

Package NDC

71335-1214-05

Product NDC: 71335-1214

Manufacturer
Bryant Ranch Prepack
Dosage Form
Tablet, Extended Release
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
March 25, 2019
Listing Expires
December 31, 2027
Application
ANDA210497
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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

71335-1214-05Selected

8 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-5)

Other packages for this product(5)

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-1)

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-2)

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-3)

120 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-4)

180 TABLET, EXTENDED RELEASE in 1 BOTTLE (71335-1214-6)