NDCFind

Bupropion Hydrochloride 71205-0465-60

Package NDC

71205-0465-60

Product NDC: 71205-0465

Manufacturer
Proficient Rx Lp
Dosage Form
Tablet, Extended Release
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
March 25, 2019
Listing Expires
December 31, 2026
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

71205-0465-60Selected

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-465-60)

Other packages for this product(2)

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-465-30)

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71205-465-90)