Strength
90; 8 mg/1; mg/1
Manufacturer
Nalpropion Pharmaceuticals LLCNDC
51267089099
Classification
Brand
Dosage Form
TABLET, EXTENDED RELEASE
Route
ORAL
Last Updated
2/22/2023
Active Ingredients
BUPROPION HYDROCHLORIDE; NALTREXONE HYDROCHLORIDEApproval Type
New Drug (NDA)
FDA Application
NDA200063On Market Since
10/22/2014
Pharmacological Classes
Aminoketone
Dopamine Uptake Inhibitors
Increased Dopamine Activity
Increased Norepinephrine Activity
Norepinephrine Uptake Inhibitors
Opioid Antagonist
Opioid Antagonists
Generic Alternatives
No alternatives available
No alternatives found with the same active ingredient, strength, and dosage form.
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