NDCFind

Bupropion Hydrochloride 31722-0068

Product NDC

31722-0068
Manufacturer
Camber Pharmaceuticals, Inc.
Dosage Form
Tablet, Extended Release
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
May 31, 2023
Listing Expires
December 31, 2027
Application
ANDA216800
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Active Ingredients

IngredientStrength
Bupropion Hydrochloride200 mg/1

Drug Class

Aminoketone [EPC]Dopamine Uptake Inhibitors [MoA]Increased Dopamine Activity [PE]

Packaging Options(4)

100 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-068-01)

500 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-068-05)

60 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-068-60)

90 TABLET, EXTENDED RELEASE in 1 BOTTLE (31722-068-90)