NDCFind

Bupropion Hydrochloride Sr 70436-0059-22

Generic: Bupropion Hydrochloride

Package NDC

70436-0059-22

Product NDC: 70436-0059

Manufacturer
Slate Run Pharmaceuticals, Llc
Dosage Form
Tablet, Extended Release
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
November 2, 2020
Listing Expires
December 31, 2026
Application
ANDA211347
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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

70436-0059-22Selected

250 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-059-22)

Other packages for this product(3)

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-059-01)

500 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-059-02)

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (70436-059-05)