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"71610-131-60" National Drug Code (NDC)
Bupropion Hydrochloride 90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-131-60)
(Aphena Pharma Solutions - Tennessee, LLC)
NDC Code
71610-131-60
Package Description
90 TABLET, EXTENDED RELEASE in 1 BOTTLE (71610-131-60)
Product NDC
71610-131
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
20140624
Marketing Category Name
ANDA
Application Number
ANDA077285
Manufacturer
Aphena Pharma Solutions - Tennessee, LLC
Substance Name
BUPROPION HYDROCHLORIDE
Strength
300
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/71610-131-60