NDCFind

Bupropion Hydrochloride 71205-0504-30

Package NDC

71205-0504-30

Product NDC: 71205-0504

Manufacturer
Proficient Rx Lp
Dosage Form
Tablet, Extended Release
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
November 8, 2018
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

71205-0504-30Selected

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-504-30)

Other packages for this product(2)

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-504-60)

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-504-90)