NDCFind

Bupropion Hydrochloride 68788-7786-06

Package NDC

68788-7786-06

Product NDC: 68788-7786

Manufacturer
Preferred Pharmaceuticals Inc.
Dosage Form
Tablet, Extended Release
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
October 21, 2020
Listing Expires
December 31, 2027
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

68788-7786-06Selected

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7786-6)

Other packages for this product(4)

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7786-1)

30 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7786-3)

120 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7786-8)

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (68788-7786-9)