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"67767-117-60" National Drug Code (NDC)
Bupropion Hydrochloride 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (67767-117-60)
(Actavis South Atlantic LLC)
NDC Code
67767-117-60
Package Description
60 TABLET, EXTENDED RELEASE in 1 BOTTLE (67767-117-60)
Product NDC
67767-117
Product Type Name
HUMAN PRESCRIPTION DRUG
Proprietary Name
Bupropion Hydrochloride
Non-Proprietary Name
Bupropion Hydrochloride
Dosage Form
TABLET, EXTENDED RELEASE
Usage
ORAL
Start Marketing Date
20080312
Marketing Category Name
ANDA
Application Number
ANDA077475
Manufacturer
Actavis South Atlantic LLC
Substance Name
BUPROPION HYDROCHLORIDE
Strength
150
Strength Unit
mg/1
Pharmacy Classes
Aminoketone [EPC],Dopamine Uptake Inhibitors [MoA],Increased Dopamine Activity [PE],Increased Norepinephrine Activity [PE],Norepinephrine Uptake Inhibitors [MoA]
Find more :
http://www.hipaaspace.com/medical_billing/coding/national.drug.codes/67767-117-60